Deciphering and reversing tumor immune suppression.


Autoria(s): Motz G.T.; Coukos G.
Data(s)

2013

Resumo

Generating an anti-tumor immune response is a multi-step process that is executed by effector T cells that can recognize and kill tumor targets. However, tumors employ multiple strategies to attenuate the effectiveness of T-cell-mediated attack. They achieve this by interfering with nearly every step required for effective immunity, from deregulation of antigen-presenting cells to establishment of a physical barrier at the vasculature that prevents homing of effector tumor-rejecting cells and the suppression of effector lymphocytes through the recruitment and activation of immunosuppressive cells such as myeloid-derived suppressor cells, tolerogenic monocytes, and T regulatory cells. Here, we review the ways in which tumors exert immune suppression and highlight the new therapies that seek to reverse this phenomenon and promote anti-tumor immunity. Understanding anti-tumor immunity, and how it becomes disabled by tumors, will ultimately lead to improved immune therapies and prolonged survival of patients.

Identificador

http://serval.unil.ch/?id=serval:BIB_7F10396A4568

isbn:1097-4180 (Electronic)

pmid:23890064

doi:10.1016/j.immuni.2013.07.005

isiid:000330948300006

Idioma(s)

en

Fonte

Immunity, vol. 39, no. 1, pp. 61-73

Palavras-Chave #Antigen-Presenting Cells/immunology; Humans; Lymphocyte Activation/immunology; Models, Immunological; Myeloid Cells/immunology; Neoplasms/immunology; T-Lymphocytes, Cytotoxic/immunology; T-Lymphocytes, Regulatory/immunology
Tipo

info:eu-repo/semantics/review

article