pubmed-article:9448302 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:9448302 | lifeskim:mentions | umls-concept:C0042769 | lld:lifeskim |
pubmed-article:9448302 | lifeskim:mentions | umls-concept:C0021017 | lld:lifeskim |
pubmed-article:9448302 | lifeskim:mentions | umls-concept:C0021747 | lld:lifeskim |
pubmed-article:9448302 | lifeskim:mentions | umls-concept:C0332197 | lld:lifeskim |
pubmed-article:9448302 | lifeskim:mentions | umls-concept:C0206071 | lld:lifeskim |
pubmed-article:9448302 | lifeskim:mentions | umls-concept:C1817919 | lld:lifeskim |
pubmed-article:9448302 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:9448302 | pubmed:dateCreated | 1998-3-11 | lld:pubmed |
pubmed-article:9448302 | pubmed:abstractText | Ig class switching usually occurs as a consequence of cognate interactions between antigen-specific B cells and CD4(+) alphabeta T cells. Vesicular stomatitis virus (VSV) infection of immunocompetent mice induces a rapid T-independent neutralizing IgM response followed by a long-lived T-dependent IgG response. Surprisingly, alphabeta T cell-deficient (TCRalpha-/-) mice also produced neutralizing IgG antibodies when infected with live VSV or with a recombinant vaccinia virus expressing the VSV glycoprotein (Vacc-IND-G), but not when immunized with UV-inactivated VSV (UV-VSV). The neutralizing IgG responses did not require the presence of NK cells or complement, but were crucially dependent on IFN-gamma and were predominantly of the IgG2a isotype. IgG production depended on residual CD3(+) non-alphabeta T cell populations present in the TCRalpha-/- mice, which produced IFN-gamma upon in vitro stimulation. A key role for gammadelta T cells was confirmed by the fact that TCRbeta-/- mice also generated strong neutralizing IgG responses to VSV, whereas TCRbeta-/-delta-/- mice produced very low titers. The neutralizing IgG responses of TCRalpha-/- mice were accompanied by the development of memory B cells, but not by antigen-specific germinal center (GC) formation. Thus, during viral infection of alphabeta T cell-deficient mice, gammadelta T cells may provide the signals that are required for isotype switching. | lld:pubmed |
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pubmed-article:9448302 | pubmed:language | eng | lld:pubmed |
pubmed-article:9448302 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9448302 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:9448302 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:9448302 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:9448302 | pubmed:month | Feb | lld:pubmed |
pubmed-article:9448302 | pubmed:issn | 0027-8424 | lld:pubmed |
pubmed-article:9448302 | pubmed:author | pubmed-author:ZinkernagelR... | lld:pubmed |
pubmed-article:9448302 | pubmed:author | pubmed-author:OdermattBB | lld:pubmed |
pubmed-article:9448302 | pubmed:author | pubmed-author:HengartnerHH | lld:pubmed |
pubmed-article:9448302 | pubmed:author | pubmed-author:MaloyK JKJ | lld:pubmed |
pubmed-article:9448302 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:9448302 | pubmed:day | 3 | lld:pubmed |
pubmed-article:9448302 | pubmed:volume | 95 | lld:pubmed |
pubmed-article:9448302 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:9448302 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:9448302 | pubmed:pagination | 1160-5 | lld:pubmed |
pubmed-article:9448302 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:9448302 | pubmed:year | 1998 | lld:pubmed |
pubmed-article:9448302 | pubmed:articleTitle | Interferon gamma-producing gammadelta T cell-dependent antibody isotype switching in the absence of germinal center formation during virus infection. | lld:pubmed |
pubmed-article:9448302 | pubmed:affiliation | Institute of Experimental Immunology, Department of Pathology, University of Zürich, Schmelzbergstrasse 12, CH-8091, Zürich, Switzerland. kmaloy@pathol.unizh.ch | lld:pubmed |
pubmed-article:9448302 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:9448302 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
pubmed-article:9448302 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |