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Rodrigo Nalio Ramos 2x6h35

Rodrigo Nalio Ramos 2x6h35

Nosso grupo investiga o microambiente tumoral com foco no papel das células do sistema imune, como macrófagos e linfócitos T. Utilizando técnicas de transcriptoma espacial, citometria multiparamétrica e ensaios funcionais ex-vivo nosso intuito é estabelecer, em uma perspectiva espaço-tempo, qual é a localização geo-espacial e as características fenotípicas e moleculares dessas células imunes em diferentes tumores sólidos e hematológicos. Tais projetos contam com uma estreita colaboração com médicos hematologistas e patologistas e com um grupo multidisciplinar de pesquisadores e estudantes implicados em revelar novos alvos terapêuticos para o tratamento do câncer. 5ml73

Palavras-chave: Imuno-oncologia; Macrófagos; linfócitos T; Transcriptoma espacial; terapia celular.

PESQUISA

Pós-doutorado em Imuno-oncologia pelo Cordeliers Research Center, Université Paris Descartes, Sorbonne Université, Paris - França

Pós-doutorado em Imuno-oncologia pelo Center for Cancer Immunotherapy, Instituto Curie, Paris - França

Dupla titulação de Doutorado pelo Departamento de Imunologia do Instituto de Ciências Biomédicas da Universidade de São Paulo e pela Université de Lyon -1 Claude Bernard, Centre de Recherche en Cancerologie de Lyon - França

ÁREAS DE PESQUISA

INFORMAÇÕES ADICIONAIS

Prêmios e Títulos

2022 – Prêmio Académie des Sciences em Paris/França, no quesito: Les Grandes Avancées Françaises en Biologie (colaborador)

2019 –International Society of Paediatric Oncology - Odile-Schweisguth (colaborador)

2019 - Young Researcher travel grant, Institut Curie, França

2015 - Menção honrosa - Thereza Kipnis Award, Sociedade Brasileira de Imunologia - XL Congress of the Brazilian Society of Immunology

2014 - Menção honrosa - PhD Student, XXXIX Congress of the Brazilian Society of Immunology

Publicações Selecionadas v3v4a

Ramos RN, Rodriguez C, Hubert M, Ardin M, Treilleux I, Ries CH, Lavergne E, Chabaud S, Colombe A, Trédan O, Guedes HG, Laginha F, Richer W, Piaggio E, Barbuto JAM, Caux C, Ménétrier-Caux C, Bendriss-Vermare N. CD163+ tumor-associated macrophage accumulation in breast cancer patients reflects both local differentiation signals and systemic skewing of monocytes. Clin Transl Immunology. 2020 Feb 13;9(2):e1108. PMID: 32082570; PMCID: PMC7017151.

Leruste A, *Ramos RN, *Tosello J, Tauziède-Espariat A, Brohard S, Han ZY, Beccaria K, Andrianteranagna M, Caudana P, Nikolic J, Chauvin C, Niborski LL, Manriquez V, Richer W, Masliah-Planchon J, et al. Clonally Expanded T Cells Reveal Immunogenicity of Rhabdoid Tumors. Cancer Cell. 2019 Dec 9;36(6):597-612.e8. Epub 2019 Nov 7. PMID: 31708437. (*igual contribuição)

Bourdely P, Anselmi G, Vaivode K, Ramos RN, Missolo-Koussou Y, Hidalgo S, Tosselo J, Nuñez N, Richer W, Vincent-Salomon A, Saxena A, Wood K, Lladser A, Piaggio E, Helft J, Guermonprez P. Transcriptional and Functional Analysis of CD1c+ Human Dendritic Cells Identifies a CD163+ Subset Priming CD8+CD103+ T Cells. Immunity. 2020 Aug 18;53(2):335-352.e8. Epub 2020 Jun 30. PMID: 32610077; PMCID: PMC7445430.

Nader GPF, Agüera-Gonzalez S, Routet F, Gratia M, Maurin M, Cancila V, Cadart C, Palamidessi A, Ramos RN, San Roman M, Gentili M, Yamada A, Williart A, Lodillinsky C, Lagoutte E, Villard C, Viovy JL, Tripodo C, Galon J, Scita G, Manel N, Chavrier P, Piel M. Compromised nuclear envelope integrity drives TREX1-dependent DNA damage and tumor cell invasion. Cell. 2021 Sep 30;184(20):5230-5246.e22. Epub 2021 Sep 21. PMID: 34551315.

Nalio Ramos R, Missolo-Koussou Y, Gerber-Ferder Y, Bromley , Bugatti M, Núñez NG, Tosello Boari J, Richer W, Menger L, Denizeau J, Sedlik C, Caudana P, Kotsias F, Niborski LL, Viel S, Bohec M, Lameiras S, Baulande S, Lesage L, Nicolas A, Meseure D, Vincent-Salomon A, Reyal F, Dutertre CA, Ginhoux F, Vimeux L, Donnadieu E, Buttard B, Galon J, Zelenay S, Vermi W, Guermonprez P, Piaggio E, Helft J. Tissue-resident FOLR2+ macrophages associate with CD8+ T cell infiltration in human breast cancer. Cell. 2022 Mar 31;185(7):1189-1207.e25. Epub 2022 Mar 23. PMID: 35325594.

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