Long-term skin-resident memory T cells proliferate in situ and are involved in human graft-versus-host disease-Reference-Cited by-同舟云学术

Long-term skin-resident memory T cells proliferate in situ and are involved in human graft-versus-host disease

Published:2020-11-18 Issue:570 Volume:12 Page:
ISSN:1946-6234
Container-title:Science Translational Medicine
language:en
Short-container-title:Sci. Transl. Med.

Author:

Strobl Johanna¹^ORCID,Pandey Ram Vinay¹,Krausgruber Thomas²^ORCID,Bayer Nadine¹,Kleissl Lisa¹³^ORCID,Reininger Bärbel¹^ORCID,Vieyra-Garcia Pablo⁴^ORCID,Wolf Peter⁴^ORCID,Jentus Maaia-Margo¹^ORCID,Mitterbauer Margit⁵,Wohlfarth Philipp⁵^ORCID,Rabitsch Werner⁵,Stingl Georg¹^ORCID,Bock Christoph²³⁶^ORCID,Stary Georg¹²³^ORCID

Affiliation:

1. Department of Dermatology, Medical University of Vienna, 1090 Vienna, Austria.

2. CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.

3. Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, 1090 Vienna, Austria.

4. Department of Dermatology and Venereology, Medical University of Graz, 8036 Graz, Austria.

5. Department of Internal Medicine I, Hematopoietic Stem Cell Transplantation Unit, Medical University of Vienna, 1090 Vienna, Austria.

6. Department of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.

Abstract

GVHD includes an autoinflammatory host-versus-graft component from recipient-derived skin-resident memory T cells.

Funder

Austrian Academy of Sciences

Austrian Science Fund

Vienna Science and Technology Fund

Oesterreichische Nationalbank

German Foundation of Dermatology

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

Reference82 articles.

1. Cutting Edge: Tissue-Retentive Lung Memory CD4 T Cells Mediate Optimal Protection to Respiratory Virus Infection

2. Skin-resident memory CD4+ T cells enhance protection against Leishmania major infection

3. A mucosal vaccine against Chlamydia trachomatis generates two waves of protective memory T cells

4. Skin infection generates non-migratory memory CD8+ TRM cells providing global skin immunity

5. Quantifying Memory CD8 T Cells Reveals Regionalization of Immunosurveillance

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