Literature DB >> 10628768

Association between cytomegalovirus disease and chronic rejection in kidney transplant recipients.

A Humar1, K J Gillingham, W D Payne, D L Dunn, D E Sutherland, A J Matas.   

Abstract

BACKGROUND: It has long been suggested that cytomegalovirus (CMV) disease plays a role in the pathogenesis of chronic rejection (CR). However, its role has been difficult to prove, given the strong association between acute rejection and CMV, and the even stronger association between acute rejection and CR. To try to isolate the relative contribution of CMV infection in the pathogenesis of CR, we used multivariate techniques to examine risk factors for CR, including CMV disease.
METHODS: Our study population consisted of adult recipients of a first kidney graft who underwent transplantation at a single center between 1/1/85 and 6/30/97 (n = 1339).
RESULTS: Multivariate analysis using time to CR as the dependent variable demonstrated acute rejection to be the strongest risk factor (relative risk [RR] = 17.8, P = 0.0001), followed by older donor age (RR = 1.46, P = 0.01). The presence of CMV disease showed a trend toward increased risk for CR (RR = 1.30, P = 0.10), although the association was not as strong as with the other two variables. Comparing only those recipients with acute rejection and CMV disease versus those with acute rejection but no CMV disease, the relative risk of developing CR was 1.37 times higher in the former group. Recipients with acute rejection and CMV developed CR sooner and with a higher incidence versus those with acute rejection but no CMV (P = 0.002). It is interesting, however, that CMV disease was only a risk factor for CR in the presence of acute rejection. Recipients with no acute rejection and CMV disease did not have a higher incidence of CR versus those with no acute rejection and no CMV (P = NS).
CONCLUSION: CMV disease seems to play some role in the pathogenesis of CR but only in the presence of acute rejection. Reasons may include (i) the inability to adequately treat acute rejection due to the presence of CMV disease or (ii) the increased virulence of latent CMV virus in recipients being treated for acute rejection. Our data may suggest a role for more aggressive prophylaxis against CMV disease, especially at the time of treatment for acute rejection.

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Mesh:

Year:  1999        PMID: 10628768     DOI: 10.1097/00007890-199912270-00011

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  22 in total

1.  NK cell and Th17 responses are differentially induced in murine cytomegalovirus infected renal allografts and vary according to recipient virus dose and strain.

Authors:  Mao Li; Srinivasa Rao Boddeda; Bo Chen; Qiang Zeng; Trenton R Schoeb; Victoria M Velazquez; Masako Shimamura
Journal:  Am J Transplant       Date:  2018-05-07       Impact factor: 8.086

2.  Allograft rejection-related gene expression in the endothelial cells of renal transplantation recipients after cytomegalovirus infection.

Authors:  Yang Li; Hang Yan; Wu-jun Xue; Pu-xun Tian; Xiao-ming Ding; Xiao-ming Pan; Xin-shun Feng; Xiao-hui Tian; He-li Xiang; Jun Hou
Journal:  J Zhejiang Univ Sci B       Date:  2009-11       Impact factor: 3.066

3.  Subclinical viremia increases risk for chronic allograft injury in pediatric renal transplantation.

Authors:  Jodi M Smith; Lawrence Corey; Rachel Bittner; Laura S Finn; Patrick J Healey; Connie L Davis; Ruth A McDonald
Journal:  J Am Soc Nephrol       Date:  2010-07-08       Impact factor: 10.121

Review 4.  Cytomegalovirus infection and abdominal pain with mycophenolate mofetil: is there a link?

Authors:  H Gallagher; P A Andrews
Journal:  Drug Saf       Date:  2001       Impact factor: 5.606

5.  Putative episodes of T-cell-mediated rejection in patients with sustained BK viruria but no viremia.

Authors:  Kosuke Masutani; Ron Shapiro; Amit Basu; Henkie Tan; Toshiharu Ninomiya; Parmjeet Randhawa
Journal:  Transplantation       Date:  2012-07-15       Impact factor: 4.939

6.  The life cycle and pathogenesis of human cytomegalovirus infection: lessons from proteomics.

Authors:  Pierre M Jean Beltran; Ileana M Cristea
Journal:  Expert Rev Proteomics       Date:  2014-10-18       Impact factor: 3.940

7.  Cytomegalovirus-responsive γδ T cells: novel effector cells in antibody-mediated kidney allograft microcirculation lesions.

Authors:  Thomas Bachelet; Lionel Couzi; Vincent Pitard; Xavier Sicard; Claire Rigothier; Sébastien Lepreux; Jean-François Moreau; Jean-Luc Taupin; Pierre Merville; Julie Déchanet-Merville
Journal:  J Am Soc Nephrol       Date:  2014-04-17       Impact factor: 10.121

Review 8.  Adverse effects of immunosuppression in pediatric solid organ transplantation.

Authors:  Kristine S Schonder; George V Mazariegos; Robert J Weber
Journal:  Paediatr Drugs       Date:  2010       Impact factor: 3.022

Review 9.  Allograft rejection: effect of local synthesis of complement.

Authors:  Steven H Sacks; Wuding Zhou
Journal:  Springer Semin Immunopathol       Date:  2005-11-11

10.  Association of Premature Immune Aging and Cytomegalovirus After Solid Organ Transplant.

Authors:  Lauren E Higdon; Claire E Gustafson; Xuhuai Ji; Malaya K Sahoo; Benjamin A Pinsky; Kenneth B Margulies; Holden T Maecker; Jorg Goronzy; Jonathan S Maltzman
Journal:  Front Immunol       Date:  2021-05-27       Impact factor: 7.561

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