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Volume 35, Issue 2, Pages 160-166 (February 2006)


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Cytomegalovirus-specific CD4 T-cell and glycoprotein B specific antibody response in recipients of allogenic stem cell transplantation

Beatrice Ludwiga, Frank Bernhard Krausb, Melanie Kippa, Wolfgang Preisera, Rainer Schwerdtfegerc, Hans Wilhelm Doerra, Sigune BuxbaumaCorresponding Author Informationemail address

Received 19 January 2005; received in revised form 15 June 2005; accepted 17 June 2005. published online 22 August 2005.

Abstract 

Background

The human cytomegalovirus (HCMV) causes severe complications in immunosuppressed patients, resulting in increased morbidity and mortality. The immunological components important for the control of HCMV are still not completely understood.

Objective and study design

To evaluate the importance of cellular and humoral immunity in stem cell transplant (SCT) recipients, we analysed levels of HCMV specific IFN-γ producing CD4+ cells and glycoprotein B (gB) specific antibodies in HCMV positive SCT patients with and without reactivation episodes after SCT.

Results and conclusion

Patients without HCMV reactivation episodes showed a slow but steady increase in both parameters after SCT, indicating that initial high levels of gB specific antibodies or HCMV specific CD4+ IFN-γ+ cells are not necessary to prevent reactivation of HCMV. In contrast, patients with reactivation episodes showed a steep, significant increase in HCMV specific CD4+ IFN-γ+ counts just prior to HCMV reactivation, followed by a decline after the reactivation period. Patients who underwent only a single reactivation generated significant higher amounts of CD4+ IFN-γ+ cells, than did patients with further reactivation episodes. The course of gB specific antibodies for reactivating patients was different, with significantly higher average values in the patients with HCMV reactivation. This indicates that patients with a HCMV reactivation exhibit a stronger humoral dominated immune response.

a Institute for Medical Virology, Johann Wolfgang Goethe University Frankfurt, Paul Ehrlich-Str.40, D-60596 Frankfurt am Main, Germany

b Institute for Zoology, Martin-Luther-University Halle/Wittenberg, Hoher Weg 4, 06099 Halle (Saale), Germany

c Deutsche Klinik für Diagnostik, Aukammallee 33, 65191 Wiesbaden, Germany

Corresponding Author InformationCorresponding author. Tel.: +49 69 6301 83062; fax: +49 69 6301 83061.

PII: S1386-6532(05)00179-4

doi:10.1016/j.jcv.2005.06.004


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