B7 costimulatory ligand regulates development of the T-cell response to Cryptococcus neoformans.

Abstract:

:The contribution of B7 molecules to the induction and maintenance of the T-cell response to the human pathogenic fungus Cryptococcus neoformans was investigated. T-cell activation by C. neoformans was regulated by B7 molecules. This costimulatory signal was necessary for initiation and maintenance of the T-cell response, through early and late requirements for B7-CD28 interaction. Blocking B7-2 inhibited the normal T-cell proliferative response. This inhibition was due, in part, to a reduced capability of T cells to produce interleukin-2 (IL-2). In contrast, the same T-cell population produced more interferon-gamma. Suppression of the normal lymphoproliferation and IL-2 secretion responses to encapsulated C. neoformans by antibodies to B7 was largely reversed by addition of the monoclonal antibody 2H1, that is reactive with the major capsular polysaccharide, glucuronoxylomannan. Overall, our data indicate that B7 molecules play a critical role in T-cell activation by C. neoformans and suggest that appropriate manipulation could drive T helper type 1 cell development.

journal_name

Immunology

journal_title

Immunology

authors

Monari C,Kozel TR,Casadevall A,Pietrella D,Palazzetti B,Vecchiarelli A

doi

10.1046/j.1365-2567.1999.00853.x

keywords:

subject

Has Abstract

pub_date

1999-09-01 00:00:00

pages

27-35

issue

1

eissn

0019-2805

issn

1365-2567

pii

imm853

journal_volume

98

pub_type

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