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Prognostic significance of interleukin-17A-producing colorectal tumour antigen-specific T cells

Thomson, Amanda (author)
Cardiff Univ, Wales
Bento, Diana F. Costa (author)
Cardiff Univ, Wales
Scurr, Martin J. (author)
Cardiff Univ, Wales
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Smart, Kathryn (author)
Cardiff Univ, Wales
Somerville, Michelle S. (author)
Cardiff Univ, Wales
Keita, Åsa (author)
Linköpings universitet,Avdelningen för kirurgi, ortopedi och onkologi,Medicinska fakulteten
Gallimore, Awen (author)
Cardiff Univ, Wales
Godkin, Andrew (author)
Cardiff Univ, Wales; Univ Hosp Wales, Wales
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 (creator_code:org_t)
2021-03-05
2021
English.
In: British Journal of Cancer. - : SPRINGERNATURE. - 0007-0920 .- 1532-1827. ; 124:9, s. 1552-1555
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background The T cell cytokine profile is a key prognostic indicator of post-surgical outcome for colorectal cancer (CRC). Whilst T(H)1 (IFN-gamma(+)) cell-mediated responses generated in CRC are well documented and are associated with improved survival, antigen-specific T(H)17 (IL-17A(+)) responses have not been similarly measured. Methods We sought to determine the cytokine profile of circulating tumour antigen-(5T4/CEA) specific T cells of 34 CRC patients to address whether antigen-specific IL-17A responses were detectable and whether these were distinct to IFN-gamma responses. Results As with IFN-gamma-producing T cells, anti-5T4/CEA T(H)17 responses were detectable predominantly in early stage (TNM I/II) CRC patients. Moreover, whilst IL-17A was always produced in association with IFN-gamma, this release was mainly from two distinct T cell populations rather than by dual producing T cells. Patients mounting both tumour-specific T(H)1(+)/T(H)17(+) responses exhibited prolonged relapse-free survival. Conclusions Tumour antigen-specific T(H)17 responses play a beneficial role in preventing post-operative colorectal tumour recurrence.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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