Viral induction of co-stimulatory activity on antigen-presenting cells bypasses the need for CD4+ T-cell help in CD8+ T-cell responses.
Identifieur interne : 000417 ( PubMed/Corpus ); précédent : 000416; suivant : 000418Viral induction of co-stimulatory activity on antigen-presenting cells bypasses the need for CD4+ T-cell help in CD8+ T-cell responses.
Auteurs : Y. Wu ; Y. LiuSource :
- Current biology : CB [ 0960-9822 ] ; 1994.
English descriptors
- KwdEn :
- Animals, Antigen-Presenting Cells (immunology), CD4-Positive T-Lymphocytes (immunology), CD8-Positive T-Lymphocytes (immunology), In Vitro Techniques, Influenza A virus (classification), Influenza A virus (immunology), Lymphocyte Activation, Lymphocyte Cooperation, Mice, Mice, Inbred BALB C, Mice, Inbred CBA, Models, Biological.
- MESH :
Abstract
CD4+ T-cell help is critical for cytotoxic (CD8+) T-lymphocyte responses to many antigens, such as viruses, minor histocompatibility antigens and allogeneic major histocompatibility antigens. However, the nature of such help is still a mystery: cytokines such as interleukin-2 may be involved but cell-cell contact may also be necessary. As some viruses can induce CD8+ T-cell responses in the absence of CD4+ T cells, we asked whether these viruses and CD4+ cells share a pathway for helping the CD8+ T-cell response.
DOI: 10.1016/s0960-9822(00)00110-x
PubMed: 7922370
Links to Exploration step
pubmed:7922370Le document en format XML
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<author><name sortKey="Wu, Y" sort="Wu, Y" uniqKey="Wu Y" first="Y" last="Wu">Y. Wu</name>
<affiliation><nlm:affiliation>Department of Pathology, New York University Medical Center, New York 10016.</nlm:affiliation>
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<author><name sortKey="Liu, Y" sort="Liu, Y" uniqKey="Liu Y" first="Y" last="Liu">Y. Liu</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Viral induction of co-stimulatory activity on antigen-presenting cells bypasses the need for CD4+ T-cell help in CD8+ T-cell responses.</title>
<author><name sortKey="Wu, Y" sort="Wu, Y" uniqKey="Wu Y" first="Y" last="Wu">Y. Wu</name>
<affiliation><nlm:affiliation>Department of Pathology, New York University Medical Center, New York 10016.</nlm:affiliation>
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<author><name sortKey="Liu, Y" sort="Liu, Y" uniqKey="Liu Y" first="Y" last="Liu">Y. Liu</name>
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<series><title level="j">Current biology : CB</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term>
<term>Antigen-Presenting Cells (immunology)</term>
<term>CD4-Positive T-Lymphocytes (immunology)</term>
<term>CD8-Positive T-Lymphocytes (immunology)</term>
<term>In Vitro Techniques</term>
<term>Influenza A virus (classification)</term>
<term>Influenza A virus (immunology)</term>
<term>Lymphocyte Activation</term>
<term>Lymphocyte Cooperation</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Mice, Inbred CBA</term>
<term>Models, Biological</term>
</keywords>
<keywords scheme="MESH" qualifier="classification" xml:lang="en"><term>Influenza A virus</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Antigen-Presenting Cells</term>
<term>CD4-Positive T-Lymphocytes</term>
<term>CD8-Positive T-Lymphocytes</term>
<term>Influenza A virus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>In Vitro Techniques</term>
<term>Lymphocyte Activation</term>
<term>Lymphocyte Cooperation</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Mice, Inbred CBA</term>
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<front><div type="abstract" xml:lang="en">CD4+ T-cell help is critical for cytotoxic (CD8+) T-lymphocyte responses to many antigens, such as viruses, minor histocompatibility antigens and allogeneic major histocompatibility antigens. However, the nature of such help is still a mystery: cytokines such as interleukin-2 may be involved but cell-cell contact may also be necessary. As some viruses can induce CD8+ T-cell responses in the absence of CD4+ T cells, we asked whether these viruses and CD4+ cells share a pathway for helping the CD8+ T-cell response.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">7922370</PMID>
<DateCompleted><Year>1994</Year>
<Month>11</Month>
<Day>18</Day>
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<DateRevised><Year>2019</Year>
<Month>07</Month>
<Day>28</Day>
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<Article PubModel="Print"><Journal><ISSN IssnType="Print">0960-9822</ISSN>
<JournalIssue CitedMedium="Print"><Volume>4</Volume>
<Issue>6</Issue>
<PubDate><Year>1994</Year>
<Month>Jun</Month>
<Day>01</Day>
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<Title>Current biology : CB</Title>
<ISOAbbreviation>Curr. Biol.</ISOAbbreviation>
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<ArticleTitle>Viral induction of co-stimulatory activity on antigen-presenting cells bypasses the need for CD4+ T-cell help in CD8+ T-cell responses.</ArticleTitle>
<Pagination><MedlinePgn>499-505</MedlinePgn>
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<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">CD4+ T-cell help is critical for cytotoxic (CD8+) T-lymphocyte responses to many antigens, such as viruses, minor histocompatibility antigens and allogeneic major histocompatibility antigens. However, the nature of such help is still a mystery: cytokines such as interleukin-2 may be involved but cell-cell contact may also be necessary. As some viruses can induce CD8+ T-cell responses in the absence of CD4+ T cells, we asked whether these viruses and CD4+ cells share a pathway for helping the CD8+ T-cell response.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">We show here that the H2N2 subtype of influenza virus, which elicits a CD4+ T-cell-independent anti-viral CD8+ T-cell response in vitro, induces expression of the co-stimulatory molecule B7-2, but not of B7, on the cell surface of antigen-presenting cells. In contrast, the H1N1 subtype of influenza virus, which requires CD4+ T-cell help to elicit CD8+ T-cell responses under the same conditions, does not induce B7-2 expression. We also find that CD4+ T cells can induce expression of B7-2 on antigen-presenting cells. In both cases, the induced B7-2 is necessary for the clonal expansion and functional maturation of CD8+ T cells.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Our results support the view that the induction of co-stimulatory activity on antigen-presenting cells by CD4+ T cells can substitute for the requirement for exogenous interleukin-2 in CD8+ T-cell help. Viruses that can induce co-stimulatory activity on antigen-presenting cells thus induce a CD4+ T-cell-independent CD8+ T-cell response. These findings could explain the reported differences in the requirements for CD4+ T cells in CD8+ T-cell responses.</AbstractText>
</Abstract>
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<AffiliationInfo><Affiliation>Department of Pathology, New York University Medical Center, New York 10016.</Affiliation>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
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<MeshHeading><DescriptorName UI="D000938" MajorTopicYN="N">Antigen-Presenting Cells</DescriptorName>
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<MeshHeading><DescriptorName UI="D015496" MajorTopicYN="N">CD4-Positive T-Lymphocytes</DescriptorName>
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<MeshHeading><DescriptorName UI="D008213" MajorTopicYN="N">Lymphocyte Activation</DescriptorName>
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<MeshHeading><DescriptorName UI="D008808" MajorTopicYN="N">Mice, Inbred CBA</DescriptorName>
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<MeshHeading><DescriptorName UI="D008954" MajorTopicYN="N">Models, Biological</DescriptorName>
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