key: cord-0018538-oxt6bojf
authors: Denis Musquer, Marie; Jouand, Nicolas; Pere, Morgane; Lamer, Juliette Eugène; Bézieau, Stéphane; Matysiak, Tamara; Faroux, Roger; Caroli Bosc, François-Xavier; Rousselet, Marie-Christine; Leclair, François; Mosnier, Jean-François; Toquet, Claire; Gervois, Nadine; Bossard, Céline
title: High-Density of FcγRIIIA(+) (CD16(+)) Tumor-Associated Neutrophils in Metastases Improves the Therapeutic Response of Cetuximab in Metastatic Colorectal Cancer Patients, Independently of the HLA-E/CD94-NKG2A Axis
date: 2021-06-15
journal: Front Oncol
DOI: 10.3389/fonc.2021.684478
sha: f6df045a0f4b5edc39734375c8d1e721cb36defe
doc_id: 18538
cord_uid: oxt6bojf

Antibody-dependent cellular cytotoxicity (ADCC) in the anti-tumor effect of cetuximab in metastatic colorectal cancer (mCRC) is only based on the impact of FcγRIIIA (CD16) polymorphisms as predictive of therapeutic response. However, nature, density and therapeutic impact of FcγRIIIA(+) (CD16) effector cells in tumor remain poorly documented. Moreover, the inhibition of cetuximab-mediated ADCC induced by NK cells by the engagement of the new inhibitory CD94-NKG2A immune checkpoint has only been demonstrated in vitro. This multicentric study aimed to determine, on paired primary and metastatic tissue samples from a cohort of mCRC patients treated with cetuximab: 1) the nature and density of FcγRIIIA(+) (CD16) immune cells, 2) the expression profile of HLA-E/β2m by tumor cells as well as the density of CD94(+) immune cells and 3) their impact on both objective response to cetuximab and survival. We demonstrated that FcγRIIIA(+) (CD16) intraepithelial immune cells mainly correspond to tumor-associated neutrophils (TAN), and their high density in metastases was significantly associated with a better response to cetuximab, independently of the expression of the CD94/NKG2A inhibitory immune checkpoint. However, HLA-E/β2m, preferentially overexpressed in metastases compared with primary tumors and associated with CD94(+) tumor infiltrating lymphocytes (TILs), was associated with a poor overall survival. Altogether, these results strongly support the use of bispecific antibodies directed against both EGFR and FcγRIIIA (CD16) in mCRC patients, to boost cetuximab-mediated ADCC in RAS wild-type mCRC patients. The preferential overexpression of HLA-E/β2m in metastases, associated with CD94(+) TILs and responsible for a poor prognosis, provides convincing arguments to inhibit this new immune checkpoint with monalizumab, a humanized anti-NKG2A antibody, in combination with anti- FcγRIIIA/EGFR bispecific antibodies as a promising therapeutic perspective in RAS wild-type mCRC patients.

Antibody-dependent cellular cytotoxicity (ADCC) in the anti-tumor effect of cetuximab in metastatic colorectal cancer (mCRC) is only based on the impact of FcgRIIIA (CD16) polymorphisms as predictive of therapeutic response. However, nature, density and therapeutic impact of FcgRIIIA + (CD16) effector cells in tumor remain poorly documented. Moreover, the inhibition of cetuximab-mediated ADCC induced by NK cells by the engagement of the new inhibitory CD94-NKG2A immune checkpoint has only been demonstrated in vitro. This multicentric study aimed to determine, on paired primary and metastatic tissue samples from a cohort of mCRC patients treated with cetuximab: 1) the nature and density of FcgRIIIA + (CD16) immune cells, 2) the expression profile of HLA-E/ b2m by tumor cells as well as the density of CD94 + immune cells and 3) their impact on both objective response to cetuximab and survival. We demonstrated that FcgRIIIA + (CD16) intraepithelial immune cells mainly correspond to tumor-associated neutrophils (TAN), and their high density in metastases was significantly associated with a better response to cetuximab, independently of the expression of the CD94/NKG2A inhibitory immune checkpoint. However, HLA-E/b2m, preferentially overexpressed in metastases compared with primary tumors and associated with CD94 + tumor infiltrating lymphocytes (TILs), was associated with a poor overall survival. Altogether, these results strongly support the use of bispecific antibodies directed against both EGFR and FcgRIIIA (CD16)

The introduction of targeted therapies, especially monoclonal antibodies targeting epidermal growth factor receptor (EGFR), such as cetuximab, a human-mouse chimeric IgG1 antibody, in the treatment of patients with metastatic colorectal cancer (mCRC), has led to a consistent improvement in survival. RAS mutations are the only well-established predictive biomarkers of resistance to cetuximab (1) . Antibody-dependent cellular cytotoxicity (ADCC) mechanism by which Fc region of the antibody binds to the Fc gamma receptors expressed by immune cells plays a key role in the antitumor effect of IgG1 antibodies (2) , and in vitro studies demonstrated that cetuximab can mediate ADCC against several tumor cell lines (3) . Fcg receptor type IIIA (FcgRIIIA), commonly expressed on NK cells as well as on several other immune cells including gd T cells, neutrophils and monocytes/macrophages, is well known for its role in ADCC (4, 5) . More specifically, the impact of FcgRIIIA polymorphisms as a predictive factor for CRC patients treated with cetuximab suggests an important role of ADCC in cetuximab efficacy (6, 7) .

In parallel, some in vitro data based on CRC cell line demonstrated that the non-classical major histocompability complex (MHC) Class I, human leucocyte antigen E (HLA-E) expressed by tumor cells and stabilized by b2 microglobulin (b2m) co-expression, inhibits the cetuximab-mediated cellular cytotoxicity induced by natural killer (NK) cells. Indeed, Levy et al. specified that this inhibitory effect on ADCC was dependent of the direct interaction between HLA-E/b2m, overexpressed by tumor cells, and its specific inhibitory receptor, CD94/NKG2A (NK group 2 member A) expressed by NK cells (8) . HLA-E is a poorly polymorphic human MHC class Ib molecule, ubiquitously expressed at low levels on the cell surface of most tissues, whose functional expression requires its stabilization by the light chain b2-microglobulin (b2m) to form a membrane heterodimeric ligand. This ligand, aberrantly overexpressed by tumor cells in several solid tumors, interacts either with the inhibitory CD94/NKG2A receptor, or the activating CD94/ NKG2C (NK group 2 member C) receptor selectively expressed by immune cells with cytolytic functions such as NK cells, NKT (natural killer T) cells and a subset of T cells (9) . Indeed, we have previously shown that overexpression of HLA-E/b2m by tumor cells (primary tumors) characterizes a subgroup of 23% of CRC. In the tumor microenvironment of those primary HLA-E/b2m + tumors, NK cells and mostly CD8 + ab T lymphocytes preferentially expressed the inhibitory CD94/ NKG2A receptor. These two immune markers (HLA-E/b2m and CD94/NKG2A) were associated with poor prognosis (10, 11) . Besides, the CD94/NKG2A receptor, recently considered as a new inhibitory immune checkpoint that blocks the terminal cytolytic tumor-attack in the tumor microenvironment, can be blocked by the anti-NKG2A antibody, monalizumab, a therapy associated with promising clinical responses in gynecologic and head and neck refractory cancers (12) .

Altogether, these results prompted us to address for the first time in a cohort of RAS wild-type mCRC patients treated with cetuximab, on paired primary and metastatic tissue samples: 1) the nature and density of FcgRIIIA + (CD16) immune cells, 2) the expression profile of HLA-E/b2m by tumor cells as well as the density of intra-tumor CD94 + immune cells and 3) their impact on both objective response to cetuximab and overall survival.

Forty-three patients treated with cetuximab for a mCRC at the "Centre Hospitalier Universitaire" (CHU) of Nantes (n=13), Angers (n=3) and La Roche sur Yon (n=7), and at the "Hopital du Confluent" of Nantes (n= 20) between 2000 and 2015, were retrospectively included in this study. For these patients, tissues samples of both primary and matched metastatic tumors were available. Rectal carcinomas previously treated with chemo-radiotherapy were excluded from the study, as well as patients with unavailable tissue samples for immunohistochemistry and/or complementary molecular analyses. As the patients were treated before the cetuximab new indications in July 2013, only the KRAS codon 12/13 (exon 2) wild-type status was known at the time of the study. For the purpose of this study, all primary and metastatic collected tissues were re-analyzed for other RAS mutations in four additional KRAS codons (exons 3 and 4) and six NRAS codons (exons 2, 3, and 4) using HRM PCR and sequencing. Additional mutations were found in 4 patients (two 436G>A mutations in KRAS exon 4 in both primary tumor and paired metastasis, one 351A>C mutation in KRAS exon 4 in a primary tumor and one 181C>A mutation in NRAS exon 3 in a metastasis), thus resulting in 39 patients with a wild-type RAS status eligible for the current study. All patients received Cetuximab plus chemotherapy (or other cytotoxic agent) for their metastatic disease (Irinotecan n=18; FOLFIRI regimen (irinotecan + folinic acid + 5 fluorouracil combination) n=10; FOLFOX regimen (oxaliplatin + folinic acid + 5 fluorouracil combination), n=6; Camptomycine n=2, Afatinib n=1), except two patients who received Cetuximab alone. Distant metastases were defined as synchronous or metachronous according to their identification, at the time of the primary tumor diagnosis or more than 12 months after, respectively (13) .

For each patient, formalin-fixed and paraffin-embedded tissues representative of the primary tumor (37 surgical resections and 2 biopsies) and matched metastasis (26 surgical resections and 13 biopsies) were selected. Tissue samples were collected from the archives of the Department of Pathology or of each participating center, and were processed according to the guidelines of our institution and of the French Ethics Committee for Research on human tissues. The institutional board of the University Hospital of Nantes approved this study. Our tissue biocollection has been registered with the French Ministry for Higher Education and Research (DC-2014-2206) with approval from the ethic committee (CPP Ouest IV-Nantes). Our study was conducted in accordance with the Helsinki Declaration.

For the flow cytometry analysis, as no viable fresh tissues samples were available for our retrospective cohort of 39 patients, we included prospectively four successive patients who benefited from a colectomy for a CRC at the University Hospital of Nantes, and who did not receive any neoadjuvant chemotherapy or radiotherapy. A fresh tissue sample of the primary tumor was immediately dissected for flow cytometry analyses. Each patient included signed an informed consent form.

Tumor response was assessed 12 weeks after starting chemotherapy by computed tomography (CT-Scan) according to the Response Evaluation Criteria in Solid Tumors (RECIST) criteria and classified as partial response (PR), stable disease (SD) or progression disease (PD). Patients with SD or PD were defined as non-responders (14) . Overall survival (OS) was measured from the date of first diagnosis (tumor resection or biopsy) to the date of death related to CRC or to the latest follow-up, and censured at five years.

In order to precisely define the nature of FcgRIIIA + (CD16) immune cells in the tumor microenvironment of CRC, we assessed by flow cytometry the phenotype of FcgRIIIA + (CD16) cells from cell suspensions derived from four fresh primary tumors of CRC patients included prospectively. Fresh dissected tumor samples were treated as described previously (15) . Briefly, the tissue fragments were cut into small pieces (1-2 mm 2 ) at room temperature in RPMI 1640 medium (Life Technologies), and then transferred into a GentleMACS C tube (MiltenyiBiotec) for two rounds of non-enzymatic mechanical dissociation with a GentleMacsOctoDissociator (Program A.01, MiltenyiBiotec). The resulting cell suspension was filtered through a 40-µm cell strainer (Dutscher), and then centrifuged for 15 min at 600g at room temperature, and finally resuspended in RPMI 1640 before the ex-vivo flow cytometry analyses.

Immediately after fresh tumor samples dissociation, 2 × 10 5 cells were incubated in 100 µl of brilliant stain buffer (BD Biosciences) with one of the three following combinations of antibodies at saturating concentrations at 4°C for 30 min. To identify FcgRIIIA + (CD16) expressing cells in the lymphoid and myeloid tumor-infiltrating cells, the CD16-Phycoerythrin (PE) mAb (clone 3G8, BD Pharmingen) was used in association with three different combinations of antibodies: 1) CD3-Brillant Violet (BV) 421 (clone UCHT1, BD Pharmingen), TCR ab-BV510 ( c l o n e T 1 0 B 9 . 1 A -3 1 , B D P h a r m i n g e n ) , T C R g d -Allophycocyanin (APC) (clone B1, BD Pharmingen), CD8a-BV650 (clone RPA-T8, BD Pharmingen), CD4-BV786 (clone L200, BD Biosciences); 2) CD3-BV421 (clone UCHT1, BD Pharmingen), CD56-APC (clone B159, BD Pharmingen), TCRa24-BV711 (clone 6B11, BD Biosciences); and 3) CD15-APC (clone HI98/HIM1, BD Pharmingen), CD11b-BV510 (clone ICRF44/44, BD Pharmingen), CD14-PE-Cyanin 7 (clone M5E2, BD Biosciences). Dead cells were identified with the viability marker Zombie NIR (BioLegend). Following incubation, cells were washed twice in PBS with 0.1% BSA medium and finally suspended in 200 µl of PBS. Stained cells were analyzed by flow cytometry using a LSRII flow cytometer and BD Diva software (BD Biosciences). The compensation adjustments were made using the anti-mouse Ig, k/negative control compensation particle set (BD Biosciences). Flow cytometry gating strategy is depicted in Figure 1A . FcgRIIIA + (CD16) immune cells were gated in lymphoid (G1) and myeloid (G2) living cells among the lymphoid cells, NK cells and T cells were identified by their CD3 − CD56 + or CD3 + TCR ab/TCR gd expression profile, respectively. Among the myeloid cells, granulocytes and monocytes/macrophages were identified by their CD15 + CD11b + CD14 − or CD15 − CD11b + CD14 +/− phenotype.

We analyzed by immunohistochemistry, both in primary tumors and paired metastasis for each patient, the density of intraepithelial FcgRIIIA + (CD16) immune cells, as immune cells in close contact with tumor cells can be considered as the most efficient effector cells to kill tumor cells via ADCC. Immunohistochemistry was performed on full tissue sections of all tumors (except for CD94/NKG2 and NKp46 performed on 19 cases due to exhaustion of some paraffin blocks). Slides were stained with the following primary antibodies: CD16 (clone 2H7, The level of HLA-E expression, assessed by staining intensity, was compared with the paired normal colonic mucosa, as previously described (10) . Furthermore, since a heterogeneous expression of HLA-E by tumor cells in whole tissue sections was observed, the percentage of strongly positive HLA-E tumor cells was also taken into account. Accordingly, HLA-E overexpression by tumor cells was defined as more than 5% of tumor cells showing a strong staining compared with that of the normal colonic mucosa.

Clinical and pathological data, as well as the percentages of CD8 + , FcgRIIIA + (CD16), NKp46 + or CD94 + , and HLA-E/b2m overexpression by tumor cells, were entered into a database. Mann-Whitney test was used to test the relationship between the density of the different intraepithelial immune cells (CD8, NKp46, FcgRIIIA (CD16), CD94) and the tissue localization (normal colonic mucosa, primary tumor and metastases). Associations between the different immunological markers (CD8, FcgRIIIA (CD16), CD94 and HLA-E/b2m) and the objective response to cetuximab at 3 months were tested by Fisher's test. Overall survivals were estimated using Kaplan-Meier method. The log-rank test and Cox regression analyses were used to assess survival differences between groups. For all analyses, a p value<0.05 was considered significant.

The main clinicopathological features of the patients included in this study are summarized in Table 1 .

In order to precise the exact nature of tumor-infiltrating immune cells that express FcgRIIIA (CD16), a flow cytometry analysis was performed on fresh tumor tissues from surgically resected primary tumors of CRC. For this purpose, 4 non metastatic patients (1 man, 3 women; aged from 67.5 to 79 years; 2 right colon, 2 left colon; 4 adenocarcinoma NOS (3 stages II and 1 stage III) who do not receive any neoadjuvant chemotherapy or radiotherapy were included prospectively.

The nature and the absolute frequency of different FcgRIIIA + (CD16) tumor-infiltrating cell types are summarized in Table 2 and are illustrated in Figure 1A . The density of FcgRIIIA + (CD16) cells in tumors, except 1 case, is quite homogeneous representing an average of 4% among all viable cells (immune and tumor cells). The case harboring a particularly rich population of FcgRIIIA + (CD16) cells (92C-51%) corresponded to a very inflamed tumor with neutrophilic microabcess. In any case, those cells mainly corresponded to myeloid cells, i.e., granulocytes and macrophages ( Figure 1B) . Indeed, about 48% and 25% of FcgRIIIA + (CD16) immune cells featured a granulocyte-like (CD15 + CD11b + CD14 − ) or a monocyte/ macrophage-like phenotype (CD15 − CD11b + CD14 +/− ), respectively. Furthermore, we also identified FcgRIIIA + (CD16) lymphoid cells representing NK cells (3.2%-14.8%, mean 7.5%) and T lymphocytes (1.5%-16.5%, mean 7.2%), mainly corresponding to CD8 + ab T cells. We did not observe any invariant NKT cells (CD3 + TCRab + TCRa24 + ) (data not shown).

The Density of FcgRIIIA + (CD16) Intraepithelial ADCC Effector Cells (Tumor-Associated Neutrophils and Cytotoxic T Lymphocytes) Is Higher in Tumors Than in the Normal Colonic Mucosa

The flow cytometry results were confirmed by immunohistochemistry, as we also identified the different FcgRIIIA + (CD16) immune cell subtypes in the stroma (CD163 + tumor-associated macrophages (TAM), and tumor-associated neutrophils (TAN) as well as TILs identified morphologically) or in the epithelial compartment (TAN and some TIL but no CD163 + TAM). As immune cells in close contact with tumor cells can be considered as the most efficient effector cells to kill tumor cells via ADCC, we focused on the density of intraepithelial FcgRIIIA + (CD16) immune cells, identified by flow cytometry, i.e., cytotoxic CD8 + T cells, NK cells and granulocytes (corresponding morphologically to TAN). As we identified morphologically 2 subpopulations of FcgRIIIA + (CD16) intraepithelial immune cells, i.e., small mononuclear cells corresponding to T lymphocytes or NK cells, and granulocytes, we performed in parallel CD8 and NKp46 immunostainings. NKp46 + cells were very rare in tumors (around 0.03%) and mostly observed in the stroma. Thus, the majority of FcgRIIIA + (CD16) mononuclear intraepithelial cells corresponded to a fraction of CD8 + lymphocytes rather than NK cells.

The mean percentages of intraepithelial CD8 + and FcgRIIIA + (CD16) cells are summarized in Table 3 and illustrated in Figure 2 . The density of FcgRIIIA + (CD16) intraepithelial effector cells was significantly higher in tumors (primary tumors or metastasis) compared with paired normal colonic mucosa (p = 0.0001). It should be noted that the percentage of each cell type, CD8 + or FcgRIIIA + (CD16), was quite similar in the primary and paired metastatic tumors, and intraepithelial FcgRIIIA + (CD16) cells were mostly neutrophils, and to a much lower degree, lymphocytes. 15 patients who exhibited a partial response, five benefited from surgical resection of their metastases. The impact of the different intraepithelial FcgRIIIA + (CD16) immune cells on the therapeutic response to cetuximab is summarized in Table 4 . The density of intraepithelial FcgRIIIA + (CD16) lymphocytes in primary tumors did not influence the clinical response to cetuximab in primary or in metastatic tumors. However, the density of intraepithelial FcgRIIIA + (CD16) TAN (≥ 0.54%, 2 nd quartile) in metastases was significantly associated with a better response to cetuximab. Furthermore, a high density of FcgRIIIA + (CD16) intraepithelial TAN in primary tumors (>0.6%, 2 nd quartile) was associated with a better OS (median not reached vs 44.03 months; log rank test = 0.0168) (Figure 3 ).

We have previously demonstrated that about 20% of CRC aberrantly overexpressed HLA-E/b2m by tumor cells (10) . This ligand is well known to interact with the CD94/NKG2A inhibitory receptor, mainly expressed by NK cells and some CD8+ T lymphocytes. Indeed, in CRC, we have shown that this receptor is preferentially expressed by CD8 + TILs (10, 11) . Furthermore, in vitro data based on CRC cell lines showed that aberrant cell surface expression of HLA-E/b2m by tumor cells inhibits the cetuximab-mediated cellular cytotoxicity by NK cells. This cetuximab-induced lysis was restored by blocking the CD94/NKG2A inhibitory receptor (8), a finding suggesting that this inhibitory immune checkpoint interferes with ADCC mediated, at least, by NK cells. Thus, we correlated herein the expression profile of these potential ADCC regulatory molecules in both primary tumors and paired metastases with the objective response to cetuximab. HLA-E/b2m was preferentially overexpressed in metastatic tumors (12/39, 30.8%) compared with primary tumors (8/39 cases, 20.5%). Noticeably, HLA-E/ b2m overexpression profile by tumor cells was concordant between primary and paired metastatic tumors in the majority of cases (31/39, 79.5%) but discordant in 8 (20.5%) cases. Among these discordant cases, the majority (6/8 cases) featured an overexpression of HLA-E/b2m by tumor cells in metastasis only, while only 2 cases were characterized by HLA-E/b2m overexpression in primary tumor ( Figures 4A-D) . According to the expression profile of HLA-E/b2m, the therapeutic response at 3 months was not statistically different between the 2 groups of tumors HLA-E + vs HLA-E − , regardless of the tumor site considered, primary or paired metastatic ( Table 5) .

Regarding the intraepithelial CD94 + immune cell density, analyzed in 19 cases, their mean percentage in primary tumors was 0.7% ± 0.5 (ranged from 0 to 1.8%) and 0.5% ± 0.5 (ranged from 0 to 1.84%) in metastases ( Figures 4E, F) . As for HLA-E expression profile, no significant relationship was observed between the density of CD94 + intraepithelial lymphocytes and the objective response to cetuximab at 3 months, regardless of the tumor site (primary or metastatic). However, as we previously demonstrated in a first cohort of 80 patients (10), we confirmed in this new independent cohort of metastatic CRC patients, that overexpression of HLA-E/b2m by tumor cells in primary tumors was significantly associated with a worse OS (median OS 35.97 months for HLA-E + primary tumors vs 57.87 months for HLA-E − primary tumors; log rank test = 0.0012) ( Figure 5A ). In the same way, a high density of CD94 + intraepithelial lymphocytes (>0.64%, 2 nd quartile) was associated with a worse overall survival compared with primary tumors containing a low density of CD94 + intraepithelial TIL (median 39.7 months vs median not reached), although the difference was not statistically significant (log rank test, p 0.079) ( Figure 5B) . In multivariate analysis taking into account the density of FcgRIIIA + 

In situ analysis of the tumor microenvironment emerges as an important means to understand tumor progression but also to predict therapeutic response through the close interactions between tumor cells and immune cells, especially in the promising field of immunotherapies -but not exclusively -, in order to improve their therapeutic efficacy (16) . In the current study, we demonstrated for the first time, in wild-type RAS mCRC patients, a significant relationship between the density of FcgRIIIa + (FcgRIIIA + (CD16) intraepithelial TAN in close contact with tumor cells in metastases and the objective response to cetuximab. Until now, the strongest evidence supporting ADCC as a key mechanism of some monoclonal antibodies was based on studies evaluating the impact of FcgRIIIa polymorphisms on clinical response to IgG1 mAbs such as rituximab in lymphoma patients (17, 18) , trastuzumab in breast carcinomas (19) or cetuximab in colorectal carcinomas (6) . The fact that we demonstrated the therapeutic impact of the density of FcgRIIIA + (CD16) ADCC effector cells in metastases, the main target of cetuximab in mCRC, gives a decisive evidence of the importance of this mechanism of action. Furthermore, as most of our responder patients (12/15) have received chemotherapy in combination with cetuximab, the synergistic effect of chemotherapy with cetuximab treatment to increase the efficiency of ADCC effectors can be raised.

Indeed, several studies have demonstrated the major role of some chemotherapeutic drugs such as anthracyclines, cyclophosphamine, oxaliplatine, among others, to boost the anti-tumor immune response, through the induction of an immunogenic tumor cell death (20) . Moreover, in the setting of ADCC, in breast adenocarcinomas, paclitaxel seems to enhance ADCC mediated by trastuzumab by rapidly recruiting ADCC effectors from blood (21) . Interestingly, regarding the exact nature of infiltrating intraepithelial effector FcgRIIIA + (CD16) immune cells in direct contact with tumor cells, we showed that the majority of those cells corresponded to TAN and to some T cells, but very few NK cells. Indeed, we identified only scarce NKp46 + NK cells, both in primary and metastatic tumors, and their density in the whole tumor (intraepithelial compartment and stroma) assessed by flow cytometry was very low. Our results are in accordance with previous studies showing the scarcity of infiltrating NK cells in CRC (11, 22, 23) . Thus, these results suggest that intraepithelial NK cells, considered as the main effector cells in monoclonal antibodies-mediated tumor therapy, are not the major effector cell population in the setting of cetuximab-mediated ADCC in mCRC. Conversely, TAN constitute the main intraepithelial FcgRIIIA + (CD16) ADCC effector cells, that we identified in both primary and metastatic tumors. Neutrophils are known to be potent mediators of ADCC against antibody-opsonized tumor cells, by a mechanism recently identified as trogoptosis (24) . Their role in ADCC was first demonstrated in vivo in tumor-xenografted murine models treated with different monoclonal antibodies (24) . In human, their cell killing mechanisms have not yet been completely unraveled, and more generally, the FcR-expressing cell populations responsible for the mAb-induced therapeutic effects on tumors, have not been formally identified. However, neutrophils could represent a major player of ADCC as they constitutively express FcgRIII, and this receptor is the most abundant Fcg receptor expressed by neutrophils (25, 26) . Our results underscore this assumption as we showed that these myeloid cells represent the main intraepithelial cell subtype expressing FcgRIIIA + (CD16) and most importantly, their high density in metastases was associated with a better response to cetuximab. Sconnochia et al. also identified FcgRIIIA + (CD16) myeloid cells in the stroma of CRC primary tumors with a phenotype (CD33 + CD11b + CD11c + ) suitable for neutrophils (23) . Besides neutrophils, we also identified FcgRIIIA + (CD16) and GrB + (in an equal proportion) intraepithelial lymphocytes. Sconnochia et al. also identified in primary CRC tumor some FcgRIIIA + (CD16) T lymphocytes without more information concerning their precise localization in the stroma or in the epithelial compartment (23) . The FcgRIIIA + (CD16) intraepithelial lymphocytes we identified could correspond mainly to cytotoxic CD8 + T cells, as suggested by our flow cytometry data. According to this hypothesis, Bjorkstrom et al. found CD8 + ab T cells expressing FcgRIIIA (CD16) in the peripheral blood and in the liver of HCV-infected patients, and reported that these T cells displayed a late-stage effector phenotype and expressed high levels of perforin (27) .

Furthermore, it has been demonstrated that FcgRIIIA + (CD16) subset of CD8 + T cells was able to mediate ADCC ex vivo and that their number increased during a virus-specific Tcell response (28) . Altogether, our findings suggest that FcgRIIIA + (CD16) intraepithelial TAN, as well as FcgRIIIA + (CD16) intraepithelial cytotoxic T lymphocytes although found in a lower proportion than TAN, represent important ADCC effector cells in metastases in a context of cetuximab-based therapy in mCRC patients. From a clinical point of view, our results provide strong support for the use of bispecific antibody anti-EGFR/anti-FcgRIIIA as a novel strategy of antitumor immunotherapy to improve the ADCC-mediated efficiency of cetuximab in recruiting FcgRIIIA + (CD16) ADCC effector cells at tumor site and offering an effective linkage between drugs and tumor target. Indeed, a phase I study has already tested a bispecific antibody (AFM13) directed against both the FcgRIIIa (CD16) and CD30, a membrane antigen strongly expressed by tumor cells, in patients with refractory or relapsed Hodgkin's lymphoma and demonstrated its tolerability and its significant effectiveness with an overall response rate of 23% (29) . One bispecific antibody targeting both FcgRIIIA (CD16) and EGF-R has yet been constructed and humanized (30) and could be tested in mCRC patients to enhance the ADCC-mediated response to cetuximab. Interestingly, in contrast to some in vitro experiments based on co-cultures showing that HLA-E overexpression by CRC cell lines inhibits the cetuximab-mediated cellular cytotoxicity by NK cells via engagement of its inhibitory CD94/NKG2A receptor (8), we failed to demonstrate a negative impact of HLA-E/b2m overexpression by tumor cells or presence of CD94 + immune cells on the clinical response to cetuximab. These apparent discordant results could be explained by the limitation of the in vitro conditions (CRC cell lines co-cultured with healthy PBMC containing the major effectors of ADCC, i.e., NK cells), which do not mimic the CRC tumor microenvironment. Indeed, the immune cell populations recruited in CRC significantly differ from those tested in these in vitro experiments, as we detected only scarce NK cells in line with other previous studies, but numerous FcgRIIIA + (CD16) TAN which are known not to express (or scarcely) the inhibitory CD94/NKG2A receptor (31) . Thus, one can hypothesize that intra-epithelial TILs, mostly corresponding to CD8 + TILs, could replace NK cells to inhibit the cetuximab-mediated cellular cytotoxicity as they represent the second cytotoxic cell type known to display this inhibitory receptor. However, we found an altered balance between FcgRIIIA + (CD16) TAN and CD94 + intra-epithelial TILs in metastases (0.99% vs 0.5%, respectively) that could explain this lack of significant inhibitory effect on ADCC. So we can speculate that NKG2A could represent a critical player in this imbalance between TAN and CD94 + intraepithelial cytotoxic TILs, limiting the expansion of cytotoxic TILs without affecting TAN expansion, and thus, impairing the anti-tumor immune response mediated by those TILs.

In line with this defective anti-tumor immune response caused by exhausted cytotoxic TILs by the engagement of the CD94/NKG2A-HLA-E/b2m axis, we confirmed in this study, based on an independent cohort of metastatic CRC patients, our previous results demonstrating that overexpression of HLA-E/ b2m by tumor cells (10) , as well as the high density of CD94 + TILs (11), in primary tumors at diagnosis predict an unfavorable prognosis. Furthermore, our study, the first to explore and compare the expression profile of this new immune checkpoint in paired primary and metastatic tumors of mCRC patients, demonstrates that HLA-E/b2m is preferentially expressed by tumor cells in metastases compared with primary tumors. This differential expression of HLA-E between primary tumor and metastases was also reported by Sasaki et al. in gastric carcinoma (32) . Taking into account the confirmed unfavorable prognostic impact of this new inhibitory immune checkpoint NKG2A and its ligand HLA-E/b2m in terms of OS, our results provide additional arguments to consider that HLA-E/b2m overexpression by tumor cells promotes tumor progression in CRC and facilitates the metastatic dissemination through an immune escape mechanism. They also provide convincing arguments to inhibit this new immune checkpoint with monalizumab, a humanized IgG4 anti-NKG2A antibody, as a promising new therapeutic alternative in the field of immunotherapy for mCRC patients, beyond anti-PD1 therapies.

Furthermore, we found that the density of intraepithelial FcgRIIIA + (CD16) TAN in primary tumors was associated with a better prognosis in accordance with the results of Sconnochia et al. who reported the favorable prognostic impact associated with a high density of FcgRIIIA + (CD16) tumorinfiltrating myeloid cells in a large series of primary CRC tumors. However, they did not report the presence of FcgRIIIA + (CD16) TAN but of mainly large cells mostly corresponding to TAM (23) . Our finding rather supports the tumor-suppressive function of FcgRIIIA + (CD16) TAN in primary tumor at least, although in many tumors a high intratumor density of neutrophils is known to be associated with a poor prognosis, probably in line with the tumorsupportive function of some subpopulations of TAN (N2 phenotype) (33, 34) . Thus, the subpopulation of FcgRIIIA + (CD16) TAN we considered and counted for the first time to our knowledge, could rather represent neutrophils with N1 phenotype which exert their antitumor activity by the activation of different innate and adaptive immune cells including B and T lymphocytes, and dendritic cells (35) . Indeed, it is known that NK cells and CD8 + T lymphocytes can be engaged in bidirectional cross-talk with neutrophils, resulting in the regulation of the adaptive immune response (36) . Further studies are urgently needed to deeply explore in situ the complex interactions between innate and adaptive immune cells in the tumor microenvironment of CRC, owing to the identification of more accurate immune cells signatures as predictive/prognostic biomarkers.

In conclusion, we demonstrated for the first time in this study that a high density of FcgRIIIa + (CD16) intraepithelial TAN in close contact with tumor cells in CRC metastases, is associated with an improved response to cetuximab. From a therapeutic point of view, our results strongly support the use of bispecific antibodies as a dual targeting strategy, both neutralizing EGFR on tumor cells and recruiting FcgRIIIa + TAN in contact with tumor cells to boost the ADCC-mediated tumor cell lysis. Furthermore, the preferential overexpression of HLA-E/b2m in metastases associated with CD94 + TILs, provides supplementary convincing arguments to inhibit this new immune checkpoint NKG2A with monalizumab, in combination with anti-FcgRIIIA/EGFR bispecific antibodies as a promising therapeutic perspective in RAS wild-type mCRC patients to improve both ADCC and anti-tumor T cell responses.

The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.

Our tissue biocollection has been registered with the French Ministry for Higher Education and Research (DC-2014-2206) with approval from the ethic committee (CPP Ouest IV-Nantes). Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements. Except for the 4 patients included prospectively for the flow cytometry analysis who signed an informed consent.

CB and NG contributed to the study design, methodology, supervision, and manuscript draft. MM contributed to the experiments and morphological data analysis. MP contributed to the statistical analysis. CT, J-FM, FL, M-CR, and JL contributed to the tumor tissue availability and pathological annotations. SB contributed to genetic data. NJ contributed to flow cytometry analysis. TM, RF, and F-XB contributed to the clinical data availability of included patients. All authors contributed to the article and approved the submitted version. 

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We thank C. Deleine and S. Blandin from the tissue and cell imaging platform "MicroPICell" (from the Federative Structure Research Francois Bonamy (Nantes) for technical assistance.