Expression of Major Histocompatibility Complex Class I Chain–Related Molecule A, NKG2D, and Transforming Growth Factor–β in the Liver of Humans with Alveolar Echinococcosis: New Actors in the Tolerance to Parasites?
Author(s) -
ShaoLing Zhang,
Sophie Hüe,
D. Sène,
A. Penfornis,
Solange BressonHadni,
B Kantelip,
Sophie CaillatZucman,
Dominique A. Vuitton
Publication year - 2008
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/586709
Subject(s) - nkg2d , biology , immunology , transforming growth factor beta , major histocompatibility complex , immune system , pathology , transforming growth factor , cytotoxic t cell , microbiology and biotechnology , medicine , biochemistry , in vitro
Echinococcus multilocularis growth and persistent granuloma, which lead to the development of the severe parasitic disease alveolar echinococcosis (AE), might be caused by abnormal expression of stress-induced proteins, with subsequent abnormalities in T cell activation. Similar to its involvement in tumors, the NKG2D-major histocompatability complex class I chain-related molecules A and B (MICA/B) signaling system could be involved in host-parasite interactions; however, its involvement in helminthic diseases has never been studied.
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