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1. Preclinical assessment of IPH6501, a first-in-class IL2v-armed tetraspecific NK cell engager directed against CD20 for R/R B-NHL, in comparison with a CD20-targeting T cell engager.

2. Antitumor immunity induced by antibody-based natural killer cell engager therapeutics armed with not-alpha IL-2 variant

3. Intestinal microbiota signatures of clinical response and immune-related adverse events in melanoma patients treated with anti-PD-1

4. S258: IPH6501 IS A FIRST-IN-CLASS TETRASPECIFIC ANTIBODY-BASED NATURAL KILLER CELL ENGAGER THERAPEUTIC DEVELOPED FOR THE TREATMENT OF B-CELL NON-HODGKIN’S LYMPHOMAS

5. Microbiome as an Immunological Modifier

7. Anticancer immunotherapy by CTLA-4 blockade relies on the gut microbiota

8. IPH6501 Is a Novel NKp46-Targeting Tetraspecific Antibody-Based Natural Killer Cell Engager Therapeutic (ANKET) Armed with a Non-Alpha IL-2 Variant and Developed for the Treatment of CD20-Positive Malignancies

9. Chemokine receptor patterns in lymphocytes mirror metastatic spreading in melanoma

10. Dietary fiber and probiotics influence the gut microbiome and melanoma immunotherapy response

11. 851 Harnessing innate immunity in cancer therapies: the example of natural killer cell engagers

12. Abstract LB062: Efficacy of Responder-derived Fecal Microbiota Transplant (R-FMT) and Pembrolizumab in Anti-PD-1 Refractory Patients with Advanced Melanoma

13. Fecal microbiota transplant overcomes resistance to anti–PD-1 therapy in melanoma patients

14. MHC Class II Antigen Presentation by the Intestinal Epithelium Initiates Graft-versus-Host Disease and Is Influenced by the Microbiota

15. Immune responses to the microbiome tune MHC class II antigen presentation by the intestinal epithelium to control gut pathology

18. Abstract PR07: Role of the microbiota in inflammation and lung cancer

20. Melanoma and immunotherapy bridge 2015

22. Immunotherapy Bridge 2016 and Melanoma Bridge 2016: meeting abstracts

25. Immunotherapy Bridge 2016 and Melanoma Bridge 2016: meeting abstracts

26. Microbiome as an Immunological Modifier.

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