PD‐1 Analysis on CD28−CD27− CD4 T Cells Allows Stimulation‐Independent Assessment of CMV Viremic Episodes in Transplant Recipients. Issue 12 (22nd October 2013)
- Record Type:
- Journal Article
- Title:
- PD‐1 Analysis on CD28−CD27− CD4 T Cells Allows Stimulation‐Independent Assessment of CMV Viremic Episodes in Transplant Recipients. Issue 12 (22nd October 2013)
- Main Title:
- PD‐1 Analysis on CD28−CD27− CD4 T Cells Allows Stimulation‐Independent Assessment of CMV Viremic Episodes in Transplant Recipients
- Authors:
- Dirks, J.
Tas, H.
Schmidt, T.
Kirsch, S.
Gärtner, B. C.
Sester, U.
Sester, M. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="ajt12480-sec-0001" sec-type="section"> <p>Expression of the inhibitory receptor programmed death 1 (PD‐1) on cytomegalovirus (CMV)‐specific CD4 T cells defines a phenotype associated with CMV viremia in transplant recipients. Moreover, CD28<sup>−</sup>CD27<sup>−</sup> double negativity is known as a typical phenotype of CMV‐specific CD4 T cells. Therefore, the co‐expression of inhibitory receptors on CD28<sup>−</sup>CD27<sup>−</sup> CD4 T cells was assessed as a rapid, stimulation‐independent parameter for monitoring CMV complications after transplantation. Ninety‐three controls, 67 hemodialysis patients and 81 renal transplant recipients were recruited in a cross‐sectional and longitudinal manner. CMV‐specific CD4 T cell levels quantified after stimulation were compared to levels of CD28<sup>−</sup>CD27<sup>−</sup> CD4 T cells. PD‐1 and cytotoxic T lymphocyte–associated antigen 4 (CTLA‐4) expression on CD28<sup>−</sup>CD27<sup>−</sup> CD4 T cells were related to viremia. A percentage of ≥0.44% CD28<sup>−</sup>CD27<sup>−</sup> CD4 T cells defined CMV seropositivity (93.3% sensitivity, 97.1% specificity), and their frequencies correlated strongly with CMV‐specific CD4 T cell levels after stimulation (r = 0.73, p &lt; 0.0001). Highest PD‐1 expression levels on CD28<sup>−</sup>CD27<sup>−</sup> CD4 T cells were observed in patients with primary CMV viremia and reactivation (p &lt; 0.0001), whereas<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="ajt12480-sec-0001" sec-type="section"> <p>Expression of the inhibitory receptor programmed death 1 (PD‐1) on cytomegalovirus (CMV)‐specific CD4 T cells defines a phenotype associated with CMV viremia in transplant recipients. Moreover, CD28<sup>−</sup>CD27<sup>−</sup> double negativity is known as a typical phenotype of CMV‐specific CD4 T cells. Therefore, the co‐expression of inhibitory receptors on CD28<sup>−</sup>CD27<sup>−</sup> CD4 T cells was assessed as a rapid, stimulation‐independent parameter for monitoring CMV complications after transplantation. Ninety‐three controls, 67 hemodialysis patients and 81 renal transplant recipients were recruited in a cross‐sectional and longitudinal manner. CMV‐specific CD4 T cell levels quantified after stimulation were compared to levels of CD28<sup>−</sup>CD27<sup>−</sup> CD4 T cells. PD‐1 and cytotoxic T lymphocyte–associated antigen 4 (CTLA‐4) expression on CD28<sup>−</sup>CD27<sup>−</sup> CD4 T cells were related to viremia. A percentage of ≥0.44% CD28<sup>−</sup>CD27<sup>−</sup> CD4 T cells defined CMV seropositivity (93.3% sensitivity, 97.1% specificity), and their frequencies correlated strongly with CMV‐specific CD4 T cell levels after stimulation (r = 0.73, p &lt; 0.0001). Highest PD‐1 expression levels on CD28<sup>−</sup>CD27<sup>−</sup> CD4 T cells were observed in patients with primary CMV viremia and reactivation (p &lt; 0.0001), whereas CTLA‐4 expression was only elevated during primary CMV viremia (p &lt; 0.05). Longitudinal analysis showed a significant increase in PD‐1 expression in relation to viremia (p &lt; 0.001), whereas changes in nonviremic patients were nonsignificant. In conclusion, increased PD‐1 expression on CD28<sup>−</sup>CD27<sup>−</sup> CD4 T cells correlates with CMV viremia in transplant recipients and may serve as a specific, stimulation‐independent parameter to guide duration of antiviral therapy.</p> </sec> </abstract> … (more)
- Is Part Of:
- American journal of transplantation. Volume 13:Issue 12(2013)
- Journal:
- American journal of transplantation
- Issue:
- Volume 13:Issue 12(2013)
- Issue Display:
- Volume 13, Issue 12 (2013)
- Year:
- 2013
- Volume:
- 13
- Issue:
- 12
- Issue Sort Value:
- 2013-0013-0012-0000
- Page Start:
- 3132
- Page End:
- 3141
- Publication Date:
- 2013-10-22
- Subjects:
- Transplantation of organs, tissues, etc -- Periodicals
617.95 - Journal URLs:
- https://www.sciencedirect.com/journal/american-journal-of-transplantation ↗
http://www.blackwellpublishing.com/journal.asp?ref=1600-6135&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1600-6143 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ajt.12480 ↗
- Languages:
- English
- ISSNs:
- 1600-6135
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0838.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3697.xml