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Cited by 324

The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.

HLA-G2, -G3, and -G4 Isoforms Expressed as Nonmature Cell Surface Glycoproteins Inhibit NK and Antigen-Specific CTL Cytolysis

Riteau, Béatrice, Rouas-Freiss, Nathalie, Menier, Catherine, Paul, Pascale, Dausset, Jean, Carosella, Edgardo D·2001·The Journal of Immunology

Abstract

HLA-G is a nonclassical MHC class I molecule that plays a major role in maternal-fetal tolerance. Four membrane-bound (HLA-G1 to -G4) and two soluble (HLA-G5, and -G6) proteins are generated by alternative splicing. Only HLA-G1 has been extensively studied in terms of both expression and function. We provide evidence here that HLA-G2, -G3, and -G4 truncated isoforms reach the cell surface of transfected cells, as endoglycosidase H-sensitive glycoproteins, after a 2-h chase period. Moreover, cytotoxicity experiments show that these transfected cells are protected from the lytic activity of both innate (NK cells) and acquired (CTL) effectors. These findings highlight the immunomodulatory role that HLA-G2, -G3, and -G4 proteins will assume during physiologic or pathologic processes in which HLA-G1 expression is altered.

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Metadata

Authors
Riteau, B., Rouas-Freiss, N., Menier, C., Paul, P., Dausset, J., & Carosella, E. D.
Venue
The Journal of Immunology
Published
2001-04
Volume
166
Issue
8
Pages
5018-5026
ISSN
  • 0022-1767 (ISSN-L)
  • 1550-6606
OpenAlex
W1506551612
Cited by
324
References
35
FWCI
5.32
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: HLA-G2, -G3, and -G4 Isoforms Expressed as Nonmature Cell Surface Glycoproteins Inhibit NK and Antigen-Specific CTL Cytolysis. https://app.cochat.ai/papers/10.4049/jimmunol.166.8.5018
The paper
Riteau, B., Rouas-Freiss, N., Menier, C., Paul, P., Dausset, J., & Carosella, E. D. (2001). HLA-G2, -G3, and -G4 Isoforms Expressed as Nonmature Cell Surface Glycoproteins Inhibit NK and Antigen-Specific CTL Cytolysis. The Journal of Immunology. https://doi.org/10.4049/jimmunol.166.8.5018

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