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1.
Clin. transl. oncol. (Print) ; 24(8): 1478–1491, agosto 2022.
Article in English | IBECS | ID: ibc-206237

ABSTRACT

The recent discovery of CMTM6 and to a lesser extent CMTM4, two members of the chemokine-like factor (CKLF)-like MARVEL transmembrane domain-containing family, as master positive regulators of PD-L1 expression, the primary ligand of programmed cell death 1 (PD-1), on tumor and immune cells has opened new horizons for investigating the role of CMTM6/CMTM4 in different aspects of oncology including their clinical and prognostic values in different cancer types. The absence of a specific review article addressing the available results about the clinical and prognostic roles of CMTM6 alone and/or in combination with PD-L1 in cancer has encouraged us to write this paper. (AU)


Subject(s)
Humans , B7-H1 Antigen/metabolism , Neoplasms , Myelin Proteins , Prognosis
2.
Cell Immunol ; 377: 104554, 2022 07.
Article in English | MEDLINE | ID: mdl-35636065

ABSTRACT

T-cell-mediated immune responses play indispensable roles in the defense against infectious pathogens including human immunodeficiency virus type 1 (HIV-1) which can establish a persistent infection that leads to many alterations in T-cell-mediated immunity. The latter include T-cell hyperactivation and depletion, both of which are essential for disease progression. Determining the factors and mechanisms pathways that lead to such abnormalities in T-cell mediated immunity during HIV-1 infection and ascertaining how the virus is able to evade immune responses elicited by T cells are critical for understanding the pathophysiology of HIV-1 infection, which in turn, could lead to new insights that may accelerate the development of novel and effective therapeutic strategies. To this end, we addressed the roles played by HIV-1 Tat protein, one of the first proteins to be expressed, in the pathogenesis of HIV-1 infection, focusing on the pathological effects of this protein in the cellular adaptive immune response in which T cells are intimately involved.


Subject(s)
HIV Infections , HIV-1 , CD4-Positive T-Lymphocytes , Humans , tat Gene Products, Human Immunodeficiency Virus
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