The resolution of lesions induced by Leishmania major in mice requires a functional Fas (APO-1, CD95) pathway of cytotoxicity

European Journal of Immunology

Volumn 28, Issue 1, 1998, Pages 237-245

  Conceição Silva, Fatima ^a,b   Hahne, Michael ^a   Schröter, Michael ^a   Louis, Jacques ^a   Tschopp, Jürg ^a  

^a UNIVERSITY OF LAUSANNE   (Switzerland)

^b INSTITUTO OSWALDO CRUZ   (Brazil)

Author keywords

CD4+ T cell; Cutaneous leishmaniasis; Fas; Fas ligand

Indexed keywords

CD4 ANTIGEN; FAS ANTIGEN; GAMMA INTERFERON; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANTIGEN EXPRESSION; ANTIGEN PRESENTING CELL; APOPTOSIS; ARTICLE; CONTROLLED STUDY; CYTOTOXICITY; HELPER CELL; LEISHMANIA MAJOR; LEISHMANIASIS; MACROPHAGE; MOUSE; NONHUMAN; PRIORITY JOURNAL; SKIN DEFECT; WOUND HEALING;

ANIMALS; ANTIGENS, CD95; APOPTOSIS; CD4-POSITIVE T-LYMPHOCYTES; CYTOTOXICITY, IMMUNOLOGIC; DISEASE SUSCEPTIBILITY; FAS LIGAND PROTEIN; INTERFERON TYPE II; LEISHMANIA MAJOR; LEISHMANIASIS, CUTANEOUS; MACROPHAGES; MEMBRANE GLYCOPROTEINS; MICE; MICE, INBRED C3H; MICE, INBRED C57BL; MICE, INBRED MRL LPR; MICE, MUTANT STRAINS; RECOMBINANT PROTEINS; WOUND HEALING;

EID: 2642613665     PISSN: 00142980     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-4141(199801)28:01<237::AID-IMMU237>3.0.CO;2-O     Document Type: Article

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