Literature DB >> 207784

Productive infection with cytomegalovirus and herpes simplex virus in renal transplant recipients: role of source of kidney.

R F Pass, W K Long, R J Whitley, S J Soong, A G Diethelm, D W Reynolds, C A Alford.   

Abstract

Forty patients were prospectively studied for infection with cytomegalovirus (CMV) and herpes simplex virus (HSV) after renal transplantation. Although 85% had antibody to CMV and 95% had antibody to HSV prior to transplantation, excretion of CMV was found in 92.5%, usually as viruria, and HSV was recovered from 70%, most often from the oropharynx. Shedding of HSV reached a peak within the first month after transplantation when immunosuppression was most intense and then rapidly declined. In contrast, excretion of CMV was found in a greater proportion of patients during each interval up to about six months after transplantation and subsequently persisted in the majority of patients. Both serologic responses and viral isolation rates indicated more rapid activation of CMV but not of HSV in recipients of kidneys from cadavers than in patients who received kidneys from living related donors. At 60 days after transplantation, 76% of the recipients of kidneys from cadavers and only 33% of the recipients of kidneys from living, related donors had shed CMV (P = 0.003). These differences could not be accounted for by immunosuppressive treatment. Excretion of HSV was clearly associated with the time of most intense immunosuppression, but the major factor in initiation and maintenance of productive infection with CMV appeared to be the host vs. graft reaction.

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Year:  1978        PMID: 207784     DOI: 10.1093/infdis/137.5.556

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  7 in total

Review 1.  Infections in solid-organ transplant recipients.

Authors:  R Patel; C V Paya
Journal:  Clin Microbiol Rev       Date:  1997-01       Impact factor: 26.132

Review 2.  Acquisition of cytomegalovirus infection: an update.

Authors:  B A Forbes
Journal:  Clin Microbiol Rev       Date:  1989-04       Impact factor: 26.132

3.  Cell surface expression of human cytomegalovirus (HCMV) gp55-116 (gB): use of HCMV-recombinant vaccinia virus-infected cells in analysis of the human neutralizing antibody response.

Authors:  W J Britt; L Vugler; E J Butfiloski; E B Stephens
Journal:  J Virol       Date:  1990-03       Impact factor: 5.103

4.  A prospective study of cytomegalovirus and herpes simplex virus disease in renal transplant recipients.

Authors:  D P Walker; M Longson; N P Mallick; R W Johnson
Journal:  J Clin Pathol       Date:  1982-11       Impact factor: 3.411

5.  Serum beta 2-microglobulin and C reactive protein concentrations in viral infections.

Authors:  E H Cooper; M A Forbes; M H Hambling
Journal:  J Clin Pathol       Date:  1984-10       Impact factor: 3.411

6.  Samarangenin B from Limonium sinense suppresses herpes simplex virus type 1 replication in Vero cells by regulation of viral macromolecular synthesis.

Authors:  Yuh-Chi Kuo; Lie-Chwen Lin; Wei-Jern Tsai; Cheng-Jen Chou; Szu-Hao Kung; Yen-Hui Ho
Journal:  Antimicrob Agents Chemother       Date:  2002-09       Impact factor: 5.191

7.  Antiviral activity of PHA767491 against human herpes simplex virus in vitro and in vivo.

Authors:  Jue Hou; Zili Zhang; Qiang Huang; Jun Yan; Xiaohu Zhang; Xiaoliang Yu; Guihua Tan; Chunfu Zheng; Feng Xu; Sudan He
Journal:  BMC Infect Dis       Date:  2017-03-20       Impact factor: 3.090

  7 in total

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