2001
DOI: 10.1002/jmv.2111
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Autoantibody appearance in cytomegalovirus‐infected liver transplant recipients: Correlation with antigenemia

Abstract: The presence of anti-endothelial cells (AECA), smooth muscle (SMA), antinuclear (ANA) and antimitochondrial (AMA) autoantibodies, and liver/kidney microsomal antibody type 1 (LKM1) was investigated retrospectively in sera of liver transplant patients and correlated with cytomegalovirus (CMV) infection as determined by the antigenemia test and with the appearance of acute or chronic allograft rejection. Indirect immunofluorescence analysis was carried out in sequential sera from 40 liver transplant patients. Te… Show more

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Cited by 35 publications
(22 citation statements)
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“…33 This association could not be confirmed in the present study. Patients who developed AIHA after HSCT showed a poor outcome.…”
Section: Discussioncontrasting
confidence: 87%
“…33 This association could not be confirmed in the present study. Patients who developed AIHA after HSCT showed a poor outcome.…”
Section: Discussioncontrasting
confidence: 87%
“…For example, natural and anti-CD13-specific autoantibodies have been found in bone marrow transplant patients undergoing HCMV infection, and anti-CD13 Abs have been associated with the development of chronic graft-vs-host disease (4,5). Nonorganspecific autoantibodies associated with HCMV infection have also been detected in solid organ transplant recipients and may contribute to the development of acute and chronic allograft rejection (6,7). In addition, hypergammaglobulinemia, cryoglobulinemia, and autoantibody production are features of HCMV-induced mononucleosis and postperfusion syndrome (8,9).…”
Section: Ike Other Viruses Causing Persistent Infection Human CMV mentioning
confidence: 99%
“…Recipient dendritic cell antigen uptake and self-reactive T and/or B lymphocyte priming 10 triggers "autoantibody" production and immunity directed against non-major histocompatibility complex determinants. Some non-major histocompatibility complex cytoplasmic, nuclear, and matrix protein antigens [11][12][13][14] (reviewed in Graft [15][16][17][18] ) are shared by the donor and recipient, whereas others may be donor-specific.…”
Section: Immunological Considerationsmentioning
confidence: 99%