Epstein‐Barr virus‐related serology in marrow transplant recipients

Serial sera from 50 marrow transplant recipients were examined for their spectra and titers of antibodies to EBV‐specific antigens. Immediately before or after transplant, blood products passively transferred antibodies to EB viral capsid antigen (VCA) and EBV nuclear antigen (EBNA). In most recipie...

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Veröffentlicht in:International journal of cancer 1980-08, Vol.26 (2), p.151-157
Hauptverfasser: Lange, Beverly, Henle, Werner, Meyers, Joel D., Yang, Lily C., August, Charles, Koch, Penelope, Arbeter, Allan, Henle, Gertrude
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Sprache:eng
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Zusammenfassung:Serial sera from 50 marrow transplant recipients were examined for their spectra and titers of antibodies to EBV‐specific antigens. Immediately before or after transplant, blood products passively transferred antibodies to EB viral capsid antigen (VCA) and EBV nuclear antigen (EBNA). In most recipients, passively‐transferred antibodies were replaced by endogenous antibodies regardless of whether donor or recipient had EBV antibodies before transplantation. Commencement or resumption of endogenous EBV antibody production was not associated with signs of infectious mononucleosis or heterophil antibody responses. Antibodies to VCA rose to abnormally high titers, followed successively by antibody to early antigens (EA), and disproportionately low levels of anti‐EBNA. Unusually high anti‐VCA and anti‐EA levels persisted when tests of immune function returned to normal. Antibodies to other herpes group viruses showed no consistent changes. We conclude that (1) EBV does not cause significant clinical problems in marrow transplant recipients; (2) persistent EBV infection can become established or reestablished in the presence of antibodies to EBV; (3) marrow transplant recipients show the same exaggerated immune response to EBV as other immunodeficient patients; and (4) the pattern of EBV‐specific antibodies may be a more sensitive measure of defective cell‐mediated immunity than most conventional tests of immune function.
ISSN:0020-7136
1097-0215
DOI:10.1002/ijc.2910260205