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In vivo study of T-cell responses to skin alloantigens in Xenopus using a novel whole-mount immunohistology method.

In vivo study of T-cell responses to skin alloantigens in Xenopus using a novel whole-mount immunohistology method. Research Abstract Details 

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  • In vivo study of T-cell responses to skin alloantigens in Xenopus using a novel whole-mount immunohistology method. Abstract Text:

    thaminda ramanayakeThaminda Ramanayake,david a l simonDavid A L Simon,john g frelingerJohn G Frelinger,edith m lordEdith M Lord,jacques robertJacques Robert,

    BACKGROUND: The African clawed frog, Xenopus, is a widely used comparative model for studying the immune response to transplantation antigens. METHODS: To better define the effector cells involved in the immune response to skin alloantigens of the frog Xenopus laevis, we have adapted a whole-mount immunohistology procedure used in mice that enables us to visualize leukocyte infiltration into unfixed transplanted skin tissues using fluorescent antibodies. We characterized the leukocyte populations present in donor skin at different times after transplantation using anti-class II and CD8 monoclonal antibodies. RESULTS: In autografts, only class II Langerhans or dendritic-like cells and very few CD8 T cells were detected. In contrast, major histocompatibility complex (MHC) disparate skin grafts at the peak of acute rejection (seven days posttransplantation, 50% rejection of pigment cells) were infiltrated with a large number of bright class II leukocytes, the majority of which were CD8 T cells. Most of these cells were located outside blood vessels and often near areas lacking pigmentation. Compared to MHC-disparate skin grafts, skin differing from the host only by minor histocompatibility antigens undergoes slower (i.e., chronic) rejection; interestingly, however, it was infiltrated by similar numbers of class II and CD8 T cell effectors, but with delayed kinetics (i.e., peaked around 15 days posttransplantation). CONCLUSIONS: Our data provide direct in vivo evidence of marked infiltration of effector leukocytes, a majority of which are CD8 T cells that occurs at the onset of tissue destruction of skin allografts.

    In vivo study of T-cell responses to skin alloantigens in Xenopus using a novel whole-mount immunohistology method. Publishing Authors By Initials

    t ramanayakeT Ramanayake,da simonDA Simon,jg frelingerJG Frelinger,em lordEM Lord,j robertJ Robert,

    For similar animals: chordata: vertebrates: amphibia: anura: pipidae: xenopus: xenopus laevis research abstracts see: animals: chordata: vertebrates: amphibia: anura: pipidae: xenopus: xenopus laevis research

    PUBMED ID PMID:

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    In vivo study of T-cell responses to skin alloantigens in Xenopus using a novel whole-mount immunohistology method. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Transplantation

    VOLUME: 83

    Page Numbers: 159-66

    Journal Abbreviation: Transplantation

    ISSN: 0041-1337

    DAY: 27

    MONTH: Jan

    YEAR: 2007

    In vivo study of T-cell responses to skin alloantigens in Xenopus using a novel whole-mount immunohistology method. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 132144

    In vivo study of T-cell responses to skin alloantigens in Xenopus using a novel whole-mount immunohistology method. Keywords Mesh Terms:

    KEYWORDS: Xenopus laevis

    MESH TERMS: immunology

    Chemical & Substance for Abstract: In vivo study of T-cell responses to skin alloantigens in Xenopus using a novel whole-mount immunohistology method. Information

    Substance Name: Isoantigens

    Registry Number: 0

    Grant and Affiliation Information for In vivo study of T-cell responses to skin alloantigens in Xenopus using a novel whole-mount immunohistology method.

    AFFILIATION: Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY 14642, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIAID

    GRANT: T32-AI 07285

    ACRONYM: AI

    MEDLINETA: Transplantation

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