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Protection from Natural Killer Cell-Mediated Lysis by HLA-G Expression on Target Cells

Pazmany, Laszlo, Mandelboim, Ofer, Valés-Gómez, Mar, Davis, Daniel M., Reyburn, Hugh T., Strominger, Jack L.·1996·Science

Abstract

The outermost layer of the human placenta is devoid of classical class I human leukocyte antigens (HLA-A, HLA-B, and HLA-C) and class II proteins (HLA-DR, HLA-DQ, and HLA-DP). Although this prevents recognition by maternal T lymphocytes, the lack of class I molecules leaves these cells susceptible to attack by natural killer (NK) cells. However, trophoblast cells directly in contact with the maternal tissues express the class I molecule HLA-G, which may be involved in protecting the trophoblast from recognition by NK cells. Here evidence is provided that expression of HLA-G is sufficient to protect otherwise susceptible target cells from lysis by activated NK1 and NK2 cell lines and clones that are specific for distinct groups of HLA-C alleles. The receptors on NK cells that recognize HLA-G are also identified.

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Metadata

Authors
Pazmany, L., Mandelboim, O., Valés-Gómez, M., Davis, D. M., Reyburn, H. T., & Strominger, J. L.
Venue
Science
Published
1996-11
Volume
274
Issue
5288
Pages
792-795
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2064140853
Cited by
497
References
0
FWCI
21.76
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Protection from Natural Killer Cell-Mediated Lysis by HLA-G Expression on Target Cells. https://app.cochat.ai/papers/10.1126/science.274.5288.792
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Pazmany, L., Mandelboim, O., Valés-Gómez, M., Davis, D. M., Reyburn, H. T., & Strominger, J. L. (1996). Protection from Natural Killer Cell-Mediated Lysis by HLA-G Expression on Target Cells. Science. https://doi.org/10.1126/science.274.5288.792

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.