Inhibition of Hyperprogressive Cancer Disease Induced by Immune-Checkpoint Blockade Upon Co-Treatment with Meta-Tyrosine and p38 Pathway Inhibitor.

doi:10.21203/rs.3.rs-969535/v1

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Research Article

Inhibition of Hyperprogressive Cancer Disease Induced by Immune-Checkpoint Blockade Upon Co-Treatment with Meta-Tyrosine and p38 Pathway Inhibitor.

https://doi.org/10.21203/rs.3.rs-969535/v1

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Background

Although immune-checkpoint inhibitors (ICI) are overall promissory for cancer treatment, they entail, in some cases, an undesired side-effect called hyperprogressive-cancer disease (HPD) associated with acceleration of tumor growth and shortened survival.

Methods

To understand the mechanisms of HPD we assayed the ICI therapy on two murine tumors widely different regarding immunogenicity and, subsequently, on models of local recurrences and metastases of these tumors. To potentiate the immune response (IR), we combined ICI with meta-tyrosine - that counteracts immune-suppressive signals - and a selective inhibitor of p38 pathway that proved to counteract the phenomenon of tumor-immunostimulation.

Results

ICI were therapeutically effective against both tumor models (proportionally to their immunogenicity) but only when they faced incipient tumors. In contrast, ICI produced acceleration of large and residual tumors. The combined treatment strongly inhibited the growth of large tumors and it managed to cure 80% of mice with local recurrences and 60% of mice bearing residual metastases.

Conclusions

Tumor enhancement was paradoxically correlated to a weak increase of the antitumor IR suggesting that a weak IR – different from a strong tumor-inhibitory one - may produce stimulation of tumor growth, mimicking the HPD observed in some clinical settings.

Cancer Biology

Oncology

hyperprogressive cancer disease

immune checkpoints inhibitors

meta-tyrosine

metastases

murine tumors.

In the last 20 years, different novel immunological strategies were developed to enhance the basal anti-tumor immune response evoked by growing tumors as well as to counteract the emergence of tumor-associated negative immune-regulatory mechanisms that could down-regulate such response (1–4).

Among these strategies, blockade of immune-checkpoints has been considered the most promising one and a potential revolution for the treatment of clinical cancer (5).

This hopeful expectation is based on a large body of evidence that demonstrates that experimental growing murine tumors may be inhibited or even eradicated upon treatment with inhibitors of the cytotoxic T-lymphocyte-associated protein (CTLA)-4 and the programmed cell death-1 (PD-1)/PD ligand-1(PD-L1) pathway.

These treatments have also increased the overall survival and progression-free survival of humans affected by some cancers such as melanoma and non-small cell lung, colo-rectal, and renal cell carcinoma (6–8). However, some treated patients show no improvement and a variable fraction of them exhibits a condition called ‘hyperprogressive cancer disease’ (HPD) associated with sharp acceleration of tumor growth, worse prognosis, and shortened survival times (9–11). In addition, some initial responders eventually develop resistance to therapy, and others may be afflicted by immune-related adverse events (12).

Two main arguments could be invoked to explain the disparity between the resounding successes achieved in experimental models and the more modest results observed in clinical settings.

The first one is associated with the fact that experimental models are usually strongly immunogenic chemically-induced tumors while, in contrast, most human tumors may exhibit significantly lower immunogenicity. In support of this contention, murine tumors of spontaneous origin – which have been considered the best models for common human cancers – usually exhibit weak or undetectable immunogenicity (13–15).

The second argument is related to the fact that immune-checkpoint inhibitors (ICI) were truly effective in restraining experimental murine tumors, although only when they faced incipient tumors. Afterwards, as the tumor becomes larger, and resembles the size that could usually be detectable at first clinical inspection, null, or even stimulatory effects on tumor growth have been observed, especially when large tumors were concerned (16).

It could be argued that immunologic strategies are second-line therapies after surgery, radiotherapy, or chemotherapy have reduced tumor burden. In such cases, residual tumors associated with local recurrences or metastases may be made up of a small number of tumor cells that would mimic an incipient tumor against which ICI proved to be effective. However, despite their similarity concerning the number of cells, both incipient and residual tumors might behave utterly different in terms of their sensitivity to immunologic treatments. In effect, cells from incipient tumors are starting to grow in an otherwise healthy host while cells from a residual tumor are placed in a microenvironment that could have been drastically altered by the previous presence of a tumor.

If the arguments above mentioned were valid, the use of appropriate tumor models that closely resemble the real clinical situation might be helpful to understand – in controlled conditions - both the scope and the limitations of these anti-tumor immunologic treatments (17).

This paper has been designed:

To evaluate the efficacy of the blockade of CTLA-4 and PD-L1 immune checkpoint – and also the therapy with antitumor vaccines – in function of target immunogenicity. To this aim, we have characterized and utilized two murine tumors, a strongly immunogenic methylcholanthrene-induced fibrosarcoma (similar to those currently used to assay immunological therapies in laboratory animals) and a weakly immunogenic and highly metastatic mammary carcinoma of spontaneous origin.
To determine whether or not the inhibitory effect observed on incipient tumors upon ICI therapy is a good predictor of the outcome of this therapy on residual tumors. In this way, we have compared the efficacy of ICI on the growth of incipient, mid-, and large-sized tumors with that on the re-growth of local tumor recurrences and metastases after surgical tumor removal.
To elucidate the mechanisms underlying the accelerating effect (HPD) observed on large tumors upon ICI therapy. The phenomenon of HPD upon ICI suggests that other points of immunologic control and/or aspects not accurately explored of the antitumor immune response might play a central role in limiting the efficacy of this therapy. To account for these possibilities we have, in the first place, used meta-tyrosine (m-Tyr), an unnatural isomer of tyrosine that it has recently been demonstrated to be capable of rescuing the organism from states of immunosuppression by mechanisms different from the known ICI (18). In the second place, we have considered the possibility that the antitumor immune response may be not linear but biphasic with strong immune responses producing inhibition while weak ones inducing stimulating effects on tumor growth (Suppl. Figure 1) (16, 19, 20). In a former work (16), we have suggested that a “weak” antitumor immune response associated with some stages of tumor growth enhanced the production of chemokines aimed to recruit macrophages at the tumor site, which, upon activation of TLR4 and p38 signaling pathways, would produce growth-stimulating signals leading to an accelerated tumor growth. Based on the above considerations, we have combined herein the blockade of CTLA-4 and PD-1/PD-L1 immune-checkpoints with both m-Tyr – to boost the antitumor immune response by counteracting other points of immunologic control - and inhibitors of p38 pathway – to counteract the phenomenon of tumor immunostimulation – with the hope of enabling otherwise indolent or tumor-promoting schedules to produce inhibition of tumor growth.

Animals

Female and male BALB/c mice were bred in the Academia Nacional de Medicina de Buenos Aires facilities. They were used at 2–3 months of age and 20–25 grams of weight. Nude BALB/c mice and NOD Scid Gamma (NSG) mice were purchased from Comisión Nacional de Energía Atómica and Instituto de Biología y Medicina Experimental, Argentina, respectively. Care of mice, an early experimental endpoint and all methods were according to NIH Guide for the Care and Use of Laboratory Animals. All experimental protocols were approved by the Committee for the Care and Use of Laboratory Animals (CICUAL) of Instituto de Medicina Experimental (IMEX-CONICET, protocol N°005/15). All methods were performed in accordance with ARRIVE guidelines. Randomization was carried out by Rand() in software Excel and in vivo experiments were blinded.

Murine Tumors

LMM3 : highly metastatic mammary carcinoma, kindly provided by Dr. L. Colombo (Instituto Angel Roffo, Buenos Aires, Argentina).

MC-C: strongly immunogenic fibrosarcoma induced by the chemical 3-methylcholanthrene.

More details of tumor models and surgical procedures have been reported previously (1, 21–23). Tumor dose 50 (TD50): number of tumor cells able to grow in 50% of mice. Tumor volume was calculated as 0.4ab², where a and b are the larger and smaller diameters, respectively (21, 22). We defined incipient, mid-sized, and large-sized tumors, those whose volumes were ≤ 10 mm³, 100-400 mm^3, and > 500 mm³, respectively. The medium was RPMI 1640 (Gibco) supplemented as described (1). Tumor lysates, bone marrow-derived dendritic cells isolation, splenocytes isolation, and histological analyses were performed as previously reported (1, 24, 25). Tumor growth rate (TGR) was expressed as the increase of tumor volume per unit time = tumor volume at day B - tumor volume at day A / B – A (9–11).

Reagents

HGMB1 and HSP60 were quantified using ELISA kits from Pepro-Tech, following the manufacturer’s recommendations. TNF-α, IL-12p70, IL-10 and TGF-ß were quantified using ELISA kits from R&D Systems.

Tumor vaccination strategies

Pre-treatment with X-lethally irradiated (LI) tumor cells and pre-treatment with dendritic cells (DC) incubated with tumor lysate were carried out as reported (1, 25–27).

Drugs, ICI and radiotherapy

DL-m-tyrosine (Sigma-Aldrich) and p38 inhibitor SB202190 (Santa Cruz Biotechnology) were used as described (18, 28). JSI-124 (Indofine Chemical Company, Hillsborough, NJ), an inhibitor of STAT3; JQ1 (Sigma-Aldrich), an inhibitor of PD-L1; blocking anti-mouse PD-L1, clone 10F.9G2 and anti-mouse CTLA-4 (CD152), clone 9H10 (BioXCell), were used as reported (29–31). Treatments with vincristine and radiotherapy (2000 grades in the tumor area; Philips 250/15 radiotherapy device at 220 Kv, 14 mA) were used as described (1).

Flow cytometry

Dendritic cells were incubated with different combinations of the mAbs: anti-CD11c, anti-IAd (MHC class II), anti-CD86 and anti-CD80, following the manufacturer’s recommendations. Splenocytes, and/or tumor cells were incubated with antibodies: anti CD3, CD4, CD8, CD11b, PD-1, PD-L1 - clone MIH5 -, phosphorylated-STAT3 (pSTAT3) from Ap-Biotech, Argentina, and 5,6 Carboxi Fluorescein diacetate Succinimidyl Ester (CFSE) from Molecular Probes; Eugene, OR, USA. Fluorescence of individual cells was measured in a flow cytometer (Becton Dickinson) and was analyzed by Flowing (Software version 2.5.1, Turku Centre for Biotechnology. University of Turku, Finland). More details were given elsewhere (1).

Proliferation assays

Lymphocyte proliferation was evaluated by CFSE staining (Molecular Probes). Briefly, 1x10⁷cells/ml were suspended in 0.3% BSA/PBS. Then, 1µl of CFSE was added for each ml (0.5 µM) (Invitrogen) and cells were incubated for 15 min at 37 ºC. Cells were washed three times with complete RPMI and incubated for 5 min at 37ºC between washes. Afterward, 1x10⁵ lymphocytes were cultured in 96-well flat-bottom plates for 24, 48, or 72 h in the presence or absence of 3x10³ DC pre-treated with tumor lysates and/or m-Tyr. Then, 30000 events were collected and CFSE low expression (proliferating lymphocytes, FL-1) was analyzed by flow cytometry as described above.

Western blotting

Western blotting was carried out with standard techniques as described and analyzed by ImageQuant software. The following antibodies were used: anti–p-STAT3, anti-STAT3 (Santa Cruz Biotechnology, Paso Robles, CA), anti-p38 (Santa Cruz Biotechnology) and anti–β-actin (Cell Signaling Technology, Danvers, MA). Levels of each band were normalized with β actin densitometry units as reported (16).

Statistical analysis

Student's t-test, ANOVA, Mann Whitney U test and Kaplan–Meier estimator for survival curves were used. Values were expressed as mean ± standard error (SE). Differences were considered to be significant whenever the P-value was 0.05 or smaller.

Different properties of tumor models and preventive immunologic strategies

MC-C tumor proved to be strongly immunogenic as far as pre-treatment of mice with lethally-irradiated MC-C tumor cells or with DC stimulated with MC-C tumor lysate strongly prevented the growth of live MC-C tumor cells implanted thereafter (Figure 1A). This effect was tumor-specific and T-cell dependent (not shown), indicating specific and robust tumor antigens.

MC-C tumor immunogenicity was associated with the capacity of MC-C tumor lysate to promote the maturation of DC as evaluated by the up-regulation of cell surface receptors CD80, CD86 and MHC II as well as production of the inflammatory cytokines TNF-α and IL-12p70 (Figure 1B, C and D). In addition, this capacity of MC-C tumor lysate was correlated to its high concentration of HGMB1 and Hsp60 – two recognized danger signals that favor DC maturation – and low concentration of IL-10 and TGF-β – two known immunosuppressive cytokines that inhibit DC maturation (1, 24); (Figure 1E and F). In turn, MC-C tumor cells exhibited low constitutive expression of phosphorylated STAT3 (pSTAT3) – an activated molecule that is involved in the transcription of genes that induce tolerogenic and immunosuppressive signals (16); (Figure 2A, B and C) – and low expression of surface PD-L1 (Figure 2D, E, and G).

On the other hand, LMM3 tumor displayed weak (if any) immunogenicity (Figure 1A), which was associated with the incapacity of LMM3 tumor lysate to promote maturation of DC (Figure 1B, C and D). This incapacity was correlated to a low concentration of HGMB1 and Hsp60 and a high concentration of IL-10 and TGF-β present in LMM3-tumor lysate (Figure 1E and F). LMM3 tumor cells exhibited high constitutive expression of pSTAT3 (Figure 2A, B and C) and high expression of surface PD-L1 (Figure 2D, E and H).

The immunosuppressive properties of LMM3 tumor lysate were confirmed by its ability to counteract the capacity of LPS to promote DC maturation. In contrast, lysates prepared from normal spleen cells or MC-C tumor cells did not counteract LPS capacity (Suppl. Figure 2).

Tumor lysate prepared from LMM3 tumor cells pre-treated with a natural inhibitor of pSTAT3 called JSI-124 acquired a significant capacity to promote the maturation of DC in a dose-dependent manner (Figure 2I). In turn, pre-treatment of mice with these DC produced a significant protective effect (preventive vaccination) against the growth of live tumor cells implanted thereafter (Figure 2J). A vaccinating similar effect was achieved with lethally-irradiated LMM3 tumor cells that had been pre-treated – before being irradiated - either with JQ1 (to inhibit the expression of PD-L1 or JSI-124 (to inactivate pSTAT3). These protective effects were tumor-specific and T-cell dependent (not shown).

The above considerations suggest that both chemically-induced MC-C and spontaneous LMM3 tumors bear specific antigens. However, in LMM3, these antigens seemed to be hidden by immunosuppressive signals released by the own tumor cells. It is worth noting that, even counteracting the mechanisms that prevent the onset of an anti-LMM3 tumor immune response, the magnitude of both the maturation of DC by LMM3 lysate and the preventive vaccinations was always several orders lower than that achieved with MC-C tumor. It suggests that the strength of MC-C tumor antigens is much greater than that of LMM3 ones.

Contrasting effects of immunotherapies on growing tumors

When MC-C tumor cells were inoculated in naïve mice, tumor-bearing mice produced a significant anti-tumor immune response (although not strong enough to inhibit the growing tumor) characterized by classical markers of anti-tumor immunity (Suppl. Figure 3). This significant immune response was, in turn, correlated to a) a relatively low expression of PD-L1 on the surface of tumor-infiltrating CD11b⁺ myeloid cells (Figure 2F and G) and b) low expression of PD-1 in the surface of both T CD8⁺ and CD4⁺ splenic lymphocytes (Suppl. Figure 4).

On the other hand, when LMM3 tumor cells were inoculated in naïve mice, tumor-bearing mice produced a weak (if any) anti-tumor immune response (Suppl. Figure 3), which was correlated to a) high expression of PD-L1 on the surface of tumor-infiltrating CD11b⁺ myeloid cells (Figure 2F and H) and b) increased expression of PD-1 in the surface of both T CD8⁺ and CD4⁺ splenic lymphocytes (Suppl. Figure 4).

Based on these observations and on the fact that LMM3 tumor cells displayed a significantly higher expression of PD-L1 than MC-C tumor cells (see above Figure 2D, E, G and H), it was expected that the blockade of the PD-1/PD-L1 pathway might be more useful to treat LMM3 than MC-C growing tumors by unlocking the onset of an otherwise almost inexistent anti-tumor immune response. On the other hand, the blockade of CTLA-4 might be more beneficial to treat MC-C than LMM3 growing tumors by enhancing an ongoing anti-tumor immune response. Our experiments confirmed these expectations. However, in both models, the combined treatment with anti-CTLA-4 and anti-PD-L1 was better than each separately.

In the MC-C tumor model, vaccines based on lethally-irradiated MC-C tumor cells or DC stimulated by MC-C tumor lysate produced inhibitory effects on growing MC-C tumors somewhat similar to those achieved with ICI (Figure 3A and B).

On the other hand, no impact on growing LMM3 tumors was obtained with lethally-irradiated LMM3 tumor cells or DC stimulated with LMM3 lysate. Only the use of DC stimulated with LMM3 lysate prepared with inactivated STAT3 produced some anti-tumor effect although lower than that attained with ICI in both subcutaneous tumors and lung metastases (Figure 3C, D and E).

In summary, as shown comparatively in Figures 3A - D, the immunologic-mediated antitumor effects were stronger on the strongly immunogenic tumor (MC-C) than on the weakly immunogenic one (LMM3).

It is worth noting that the striking success of all of these immunologic treatments was achieved against incipient (≤ 10 mm³) but not larger growing tumors. In fact, in mice bearing large-sized tumors (mean volume: 650 - 800 mm³) – either strongly or weakly immunogenic – these treatments not only did not produce any inhibitory effect but an enhanced tumor growth (Figure 3A - D) while no effect was observed on metastases (Figure 3E). Attempting to get an effective treatment against these tumors, we doubled the doses of ICI. However, the results were worse than before since, upon this double dose treatment, all mice showed severe manifestations of auto-immunity and reached the experimental endpoint rapidly after the last dose (not shown).

Contrasting outcomes of immunological strategies on incipient and residual tumors

Although inefficient to inhibit mid- and large-sized tumors, the ability of ICI to restrain the growth of incipient tumors might still have great clinical potential value if it were demonstrated that residual tumors- supposedly the targets of ICI in clinical settings – would behave in the same way as incipient tumors regarding their sensitivity to immunologic treatments. To test this contention, we used two clinically relevant tumor models:

A model of local recurrence after subcutaneous (s.c.) MC-C tumors (650-800 mm³) were surgically excised, leaving intact the underlying skin. In these conditions, recurrent tumors become apparent one week after surgery in 100% of cases.
A model of lung metastases after s.c. LMM3 tumors (650-800 mm³) were radically removed together with the underlying skin when spontaneous metastases were already established in the lung. Local tumors do not re-grow in these conditions, but all mice die with multiple metastases within a month after surgery.

As shown in Figure 3F and G, the growth of local recurrences and metastases was not inhibited by the very same treatments that strongly inhibited the growth of incipient tumors. Actually, the development of local tumor recurrences upon treatment with ICI was enhanced in the same way as large-sized tumors – from which residual tumors were derived by surgical debulking (Figure 3F) – while the growth of metastases was similar in both treated and control groups (Figure 3G).

Simultaneous enhancement of large-sized tumors and inhibition of secondary tumor implants upon treatment with immune-checkpoint inhibitors

Enhancement of large-sized and residual tumors upon treatment with ICI and vaccines could be explained, at first sight, by an immunotherapy-mediated down-regulation of the antitumor immune response produced at the local tumor area (9, 32). If this were the case, the growth rate of such enhanced tumors could get close to that attained in constitutive immune-deficient nude and NSG mice, but actually, it was significantly higher than in the latter (Suppl. Figure 5). These results suggested that other explanations were necessary. We evaluated the immunologic state of mice bearing large-sized tumors after treatment with ICI to account for this fact. Tumor-bearing mice produced an anti-tumor immune response (Suppl. Figure 3) but only up to tumor volume reached 500 mm³. Afterwards, such immune response – either significant (for MC-C) or weak (for LMM3) – was sharply down-regulated.

A simple and reliable in vivo marker of anti-tumor immunity is the “concomitant immunity” phenomenon by which tumor-bearing mice are resistant to secondary tumor implants by a specific T-cell dependent mechanism (see Suppl. Figure 3). As shown in Figure 4A-D, upon treatment with anti-CTLA-4 and anti-PD-L1, “concomitant immunity” was partially recovered in large-sized tumor-bearing mice. Another marker of anti-tumor immunity, such as tumor-antigen specific splenic T-cell proliferation, was also partially recovered upon treatment (Figure 4E - G). In same way, after ICI therapy, percentage of splenic CD4⁺ and CD8⁺ T cells increased 16% and 32%, respectively, and, reciprocally, CD25⁺/FOXP3⁺ T regs dropped 31%.

Consequently, the enhancement of large-sized tumors upon treatment with ICI was, as paradoxical as it could be, associated with an increased anti-tumor immune response.

The stimulation of tumor growth by a relatively weak immune response has been claimed to be associated with the activation of TLR-4 and p38 pathway in macrophages attracted to the tumor place (16).

Confirming that claim, macrophages collected surrounding large-sized tumors from mice treated with ICI exhibited a significantly higher expression of p38 than that found in similar-sized tumors from non-treated mice or surrounding secondary tumor implants (Figure 4H and I).

Meta-tyrosine and blockade of p38 pathway enable an efficient anti-tumor therapy with anti-tumor vaccines and checkpoint inhibitors

Acceleration of tumor growth upon vaccines and ICI treatments might be counteracted by using two different but complementary strategies: a) SB 202190, a selective inhibitor of p38, to counteract the phenomenon of tumor-immune-stimulation; b) meta-tyrosine (m-Tyr), which, according to previously reported results (18) might restrain putative immune-checkpoints not counteracted by classical ICI and, in consequence, to act as an adjuvant for such immunologic therapies. The recovery effect of m-Tyr on splenic T-cell proliferation in immunosuppressed mice is shown in Suppl. Figure 6.

As shown in Figure 5A and B, the combined treatment not only counteracted the tumor enhancement effect by ICI but also achieved significant inhibition of large-sized tumors in both strongly and weakly immunogenic models. Antitumor vaccines produced similar effects to ICI, especially in the strongly immunogenic model. Furthermore, the combined treatment of ICI or vaccines with meta-tyrosine, and SB 202190 was even more effective than classical chemotherapy and radiotherapy against growing murine tumors (Figure 5A). However, despite these promissory results, the tumors continued to grow – although significantly more slowly than controls – and all mice finally reached the experimental endpoint.

A more striking effect was attained against the growth of local recurrences and metastases after surgical debulking the primary tumor. In effect, while local recurrences and residual metastases caused the death of 100% of non-treated controls or mice treated with each immunologic strategy separately, the combined treatment not only produced tumor-inhibitory effects but even it managed to cure about 80% of mice bearing local recurrences and about 60% of mice bearing residual metastases in the lung (Figure 5C - F and 6). It is worth noting that, in all the schedules used herein, neither m-Tyr nor SB 202190 produced, on their own, any inhibitory effect but collaborate to make powerfully efficient an otherwise inefficient therapy with vaccines and ICI.

In the last 50-60 years, surgery, radio, and chemotherapy have improved the management of human cancer. However, the progress has been much slower than initially expected, mainly associated with the difficulty of treating local recurrent and disseminated cancer. In effect, when a tumor is relatively small, and metastases are absent, cancer could be cured surgically, and 5-years survival rates are estimated at about 90%. On the other hand, when a tumor has not completely excised or it has spread to different sites, those rates often fall below 15% (33). The true problem is that there is no assurance that a localized cancer will not recur or may be listed as “before metastases” because the number of both remaining local and metastatic tumor cells after surgery may be below the limit of detection by current technology (34).

Limitations of conventional chemotherapeutic drugs to restrain both local recurrent and disseminated tumor cells are associated with its poor aqueous solubility, its lack of tumor-specificity, and the risk of multidrug resistance (35). In this context, immunologic strategies mainly based on the blockade of immune-checkpoints, emerged as a real possibility to treat advanced cancer because they could theoretically overcome the limitations of conventional non-tumor specific anti-cancer therapies.

However, although immune-checkpoint inhibitors (ICI) improved the results achieved with conventional therapies on some clinical tumors, up to date, the overall benefits are supported by a relatively small percentage of patients. Contrastingly, many of them exhibit no significant improvement or even a condition called “hyperprogressive cancer disease” (HPD) with rapid tumor growth, increased metastatic load, and shorter survival times (10, 36). It means that, once HPD occurs, ICI are not only invalid for tumor treatment but also detrimental for patients. Across studies, the incidence of HPD among immunotherapy cases ranges from 9-30%, and some lines of evidence suggest that these rates might have been underestimated (32, 36).

Based on these clinical results, it seems to be necessary not only to develop predictors of response to immunotherapy and rational combination therapies that can enhance their efficacy but also to elucidate the mechanisms underlying the phenomenon of HPD.

To this aim, in this work, we have assayed the therapy with anti-CTLA-4 and anti-PD-L1, as well as with classical antitumor vaccines, on two growing murine tumors with widely different degrees of immunogenicity, a strongly immunogenic chemically-induced fibrosarcoma and a weakly immunogenic and highly metastatic mammary adenocarcinoma of spontaneous origin. Treatment was initiated at various stages of tumor growth and assayed on the re-growth of residual tumors (local recurrences and metastases) after surgical tumor extirpation to mimic real clinic situations.

The immunological properties of both tumors, which defined their degree of immunogenicity, were previously elucidated. Pre-treatment with anti-tumor vaccines based on lethally-irradiated tumor cells or dendritic cells (DC) incubated with tumor lysate strongly prevented the challenge with live tumor cells from the chemically-induced fibrosarcoma but not from the spontaneous mammary tumor. To achieve a moderate preventive effect against the latter, tumor lysate and lethally-irradiated tumor cells needed to be pre-treated, with an inhibitor of PD-L1 or pSTAT3. These results suggested that both tumors bore specific-tumor antigens. However, in the case of the spontaneous tumor, these antigens were not only hidden but intrinsically weaker than those of the chemically-induced tumor.

The immunogenic strength of each tumor was also correlated to the antitumor immune response evoked when tumor cells were inoculated into naïve mice. In effect, mice bearing the chemically-induced tumor developed a significant antitumor immune response while mice bearing the spontaneous tumor induced a very low one. In both cases, the immune response was increased upon treatment with anti-tumor vaccines and, more efficiently, with a combination of anti-CTLA-4 plus anti-PD-L1 antibodies. This was reflected in an inhibition of both growing tumors proportionally to tumor immunogenicity.

However, even though vaccines and ICI were effective in restraining the growth of both strongly and weakly immunogenic growing tumors, they were genuinely efficient only when they faced incipient tumors (< 10 mm³). Afterwards, no anti-tumor effects were attained. In fact, when treatment started at the time when tumor was large (> 500 mm³), enhancement of tumor growth was achieved in both tumor models. In addition, when treatments were assayed on residual local tumors after surgical large tumor excision, the growth of residual tumors was enhanced in the same way as large-sized tumors from which they were derived. Regarding metastases, neither inhibitory nor stimulatory effects were observed upon treatment. These results indicated that a residual tumor, even composed of a similar number of cells to that of an incipient tumor, behaves, concerning its sensitivity to immunologic strategies, much more like a large than an incipient tumor. As a corollary, data suggest that incipient tumors are not good models to predict the outcome of immunological therapies on residual tumors.

The lack of therapeutic response or even an accelerated growth of non-incipient murine tumors after these immunologic treatments may be paralleled with the lack of response, or the HPD observed in some patients with advanced cancer who have received a therapy with ICI. The mechanisms underlying these undesired therapeutic responses remain speculative. Recent work supports the idea that HPD after therapy with ICI may be more frequent in patients with MDM2 family amplification and EGFR aberrations than patients without them (37). Another work identified increased expression of oncogenic pathways and mutations in known tumor suppressor genes such as VHL and TSC2 in tumor cells displaying HPD after therapy with anti-PD-1 therapy (38). Others have proposed that, even though treatment with anti-PD-1/PD-L1 and anti-CTLA-4 antibodies would usually expand anti-tumor CD8+ and CD4+ T cells, such treatment might, upon certain circumstances, increase the population of PD-1+ T regs producing an effect of immunosuppression. Kamada et al. (39) found that in non-HPD patients, the ratio of T-regs/CD8+ cells, the proportion of Ki67+ T-regs/ Ki67+ CD8+ cells and the percentage of Ki67+ T-regs decreased significantly after nivolumab treatment. At the same time, they remained stable or even reduced in HPD patients. In fact, PD-1+ Tregs and especially M2-like macrophage infiltration induced by anti-PD-1 antibodies have been recently considered a major hallmark of HPD in clinical settings (10, 11). In the same line, a correlation between decreased immunogenicity and HPD has been proposed (40).

Although all of the predictors and mechanisms suggested above may play a role in some cases, it is difficult to attribute to them a general role. In effect, in our experiments, differences associated with different genetic backgrounds in the tumor-bearing host are unlikely since all tumor-bearing hosts were inbred mice. In addition, the tumors that displayed hyperprogressive growth upon therapy with ICI behaved like “normal” tumors (that is, not HPD tumors) when they were transplanted into naïve mice, suggesting that no mutations occurred before or during the phase of accelerated tumor growth. In the same way, if a state of immunosuppression were the explanation for the tumor-accelerating effect produced by immunologic strategies on large or local recurrent tumors, the growth of such tumors could get relatively close to that attained in immune-depressed nude and extremely immune-deficient NSG mice but not to grow faster than the latter as it actually occurred. Further, the enhancement of large-sized and residual tumors upon immunological treatments was achieved, surprisingly, in the face of an increased anti-tumor immune response. Lastly, although low immunogenicity may favor HPD in some cases, in this work, accelerated tumor growth after immunologic treatment was observed associated with both strongly and weakly immunogenic tumors.

A putative explanation for the acceleration of tumor growth upon current immunological therapies might be attained on the basis of the theory of tumor-immunostimulation, stated by Prehn many years ago (19). That theory postulates that the antitumor immune response would not be linear, as the orthodoxy predicts, but biphasic with “strong'' immune responses producing inhibition, “weak” responses inducing acceleration of tumor growth and “very weak” ones producing no effect (see the Suppl. Figure 1 for a better understanding of the phenomenon). This proposal suggests that immunotherapy against cancer may produce, in the highly immunosuppressive microenvironment of large tumors, weak immune responses that would promote rather than inhibit tumor growth (16, 19, 27, 41). In effect, when tumors have surpassed the critical volume of 500 mm³, tumor-bearing mice usually enter into a state of systemic immune-depression against tumor antigens historically known as “immunological eclipse” that, according to our observations concerning the kinetics of the primary tumor and secondary tumor implants, would be more robust near the primary tumor than anywhere else on the body. That state of immunosuppression is presumably not reversed by incomplete surgical resection because, as we pointed above, recurrences behave, as for their sensitivity to immunologic treatments, much like the large tumors from which they were derived. At that tumor stage, the magnitude of the antitumor immune response near the tumor site could be considered, before any immunologic treatment, as “very weak” and placed near “0” on the biphasic antitumor immune response curve (see Suppl Figure 1). When an immunologic treatment is utilized against these large tumors (and also against local recurrences), it would produce a relatively weak increase of the immune reaction, moving it to the right on the curve, for example toward “c”, producing accelerated tumor growth. The observation that metastases from large tumor-bearing mice were neither inhibited nor stimulated upon the very same immunologic treatments that accelerated the primary tumor could be similarly explained by assuming that the state of immunosuppression is less profound far from the primary tumor, where metastases would be established. In consequence, in such places, the basal antitumor immune response would be, for example, near “a” and after the immunologic treatment it would be similarly increased as before, moving the immune response towards “e”, where neither inhibitory nor stimulatory effects are expected.

Although antitumor vaccines and ICI did not produce on their own inhibitory effects on large tumors or their metastases, more stringent strategies, for example by incorporating new and potent adjuvants to the treatment, could move the immune reaction beyond the stimulatory zone up to the inhibitory part of the curve (for example near “f”). In our experiments this role was achieved by meta-tyrosine (m-Tyr), an unnatural isomer of tyrosine. Former experiments had demonstrated that high concentrations of m-Tyr, chronically administered by the intravenous route, could directly inhibit tumor cell proliferation through inactivation of pSTAT3 and down-regulation of both the NFκB/NOTCH axis and survivin expression (22, 42). More recent experiments demonstrated that m-Tyr, when administered once or few times by the intraperitoneal route, as it was used herein, does not produce any direct antitumor effect but it may boost the overall immune response against different antigens and rescue the organism from states of immunosuppression not counteracted by anti-CTLA-4 and anti-PD-L1 antibodies (18). On this basis, when we combined this schedule of m-Tyr with antitumor vaccines or ICI, a significant inhibitory effect on non-incipient tumors was observed.

Another strategy to overcome the limitations of current immunologic therapies could involve the counteraction of the proper phenomenon of tumor immunostimulation. This phenomenon has recently received a mechanistic interpretation (16) according to which a weak antitumor immune response would promote tumor growth upon enhanced activation of p38 signaling pathway in macrophages recruited at the tumor site. The fact that tumor infiltration by M2 macrophages is a common finding in clinical cancer displaying HPD after treatment with ICI (10) further supports the putative involvement of the phenomenon of tumor immunostimulation in those cases. On this basis, when we combined vaccines or ICI with a specific inhibitor of p38, a significant inhibitory effect on large tumors was observed. In former works (1, 16), immunotherapeutic strategies were reported to be improved by the use of non-specific anti-inflammatory agents such as indomethacin or low doses of dexamethasone. However, in our assays the anti-inflammatory agent SB202190, specific against p-38, rendered better results.

In our hands, the best therapeutic results were accomplished by combining ICI with both m-Tyr and SB202190 to treat local tumor recurrences and metastases after surgery. This combined therapy produced a profound inhibition of the tumor growth that resulted in 80% of cures of local recurrent tumors from the strongly immunogenic tumor, and in about 60% of cures of metastatic residual tumors from the weakly immunogenic one, in a context where, no treatment produced 100% of deaths in both cases and treatment with ICI alone produced not only 100% of deaths but also hyperprogressive or accelerated tumor growth in the case of local recurrent tumors. It is worth to note that the combined therapy utilized in this work was significantly better not only than current immunologic approaches but also than conventional chemotherapy and radiotherapy. The fact that neither m-Tyr nor the specific inhibitor of p38 pathway alone produced any antitumor effect suggested that they did not act on their own but they collaborate with the current immunologic therapies allowing an otherwise ineffective immunologic strategy to have a chance to be effective. In clinical trials for advanced cancer, ICI and other immunologic approaches only evidenced significant beneficial effects in a limited cluster of patients (43–46). We suggested that these patients might exhibit stronger immune reactions than the general population or, alternatively, they have been unable to mount a significant macrophage-related-pro-tumorigenic TLR-4 and p-38 dependent inflammatory response preventing the emergence of a state of immunostimulation. The observation presented in a former paper (16) that the immunostimulatory arm of the immune response curve was not observed in Winn assays carried out in macrophage-depleted and TLR-4 knock-out mice, seems to support this suggestion. In fact, the therapeutic antitumor success (when it occurred) of BET (bromo-domain and extra-terminal motif) inhibitors could be associated, at least in part, with their ability to impair macrophage-mediated inflammation (44).

In summary, there is great interest in developing methods and markers that can identify patients and tumor types that could get benefit from different schedules of immunotherapy. In fact, hundreds of trials have been initiated in the last few years and many of them are still ongoing including ICI or new cancer vaccines either working alone or combined with chemotherapy, radiation therapy, targeted therapy, intra-tumoral therapy, novel immunomodulators, bispecific and multispecific antibodies, microbioma modulators, adoptive cell therapy including chimeric antigen T-cell receptors and other novel strategies (45, 46). In this context, the analysis of genetic profile of tumor antigens, the search for new adjuvants that can blockade new checkpoints not counteracted by already known ICI (m-Tyr is an example of them) and a deeper understanding of the phenomenon of tumor immunostimulation could also contribute to improve the current therapies against cancer.

CFSE: Carboxi Fluorescein diacetate Succinimidyl Ester

CICUAL: Committee for the Care and Use of Laboratory Animals

CTLA-4: cytotoxic T-lymphocyte-associated protein

DC: dendritic cells

HPD: hyperprogressive-cancer disease

ICI: immune-checkpoint inhibitors

IR: immune response

m-Tyr: meta-tyrosine

NSG: NOD Scid Gamma

PD-1: programmed cell death-1

PD-L1: PD ligand-1

TD50: Tumor dose 50

TGR: Tumor growth rate

Ethics approval and consent to participate

All methods were according to NIH Guide for the Care and Use of Laboratory Animals. All experimental protocols were approved by the Committee for the Care and Use of Laboratory Animals (CICUAL) of Instituto de Medicina Experimental (IMEX-CONICET, protocol N°005/15). All methods were performed in accordance with ARRIVE guidelines.

Consent for publication

Not applicable.

Availability of data and materials

All data generated or analysed during this study are included in this published article and its supplementary information files.

Competing interests

The authors declare that they have no competing interests.

Funding

This work was supported by the CONICET (PIP 112201 201006 28CO) and the Agencia Nacional de Promoción Científica y Tecnológica, (ANPCyT PICT 1590-2014).

Authors' contributions

DM performed most of the experiment and helped in writing and correcting the main manuscript text. AD collaborated with the correction of the work and together with PC helped in the accomplishment of some experiments related to figures 1 and 2. BR and MV collaborated with some experiments of figures 1 and 4. OB helped in the design and realization of in vivo experiments. RR designed and supervised all experiments and drafted the manuscript.

Acknowledgements

We thank the Centro de Investigaciones sobre Porfirinas y Porfirias (CIPYP) of the Hospital de Clínicas for their collaboration with in vivo experiments.

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Inhibition of Hyperprogressive Cancer Disease Induced by Immune-Checkpoint Blockade Upon Co-Treatment with Meta-Tyrosine and p38 Pathway Inhibitor.

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Abstract

Background

Methods

Results

Conclusions

Figures

Background

Materials And Methods

Animals

Murine Tumors

Reagents

Tumor vaccination strategies

Drugs, ICI and radiotherapy

Flow cytometry

Proliferation assays

Western blotting

Statistical analysis

Results

Different properties of tumor models and preventive immunologic strategies

Contrasting effects of immunotherapies on growing tumors

Contrasting outcomes of immunological strategies on incipient and residual tumors

Simultaneous enhancement of large-sized tumors and inhibition of secondary tumor implants upon treatment with immune-checkpoint inhibitors

Meta-tyrosine and blockade of p38 pathway enable an efficient anti-tumor therapy with anti-tumor vaccines and checkpoint inhibitors

Discussion

Abbreviations

Declarations

References

Additional Declarations

Supplementary Files

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