4.5 Article

Choice of Immunosuppression Influences Cytomegalovirus DNAemia in Cynomolgus Monkey (Macaca fascicularis) Islet Allograft Recipients

期刊

CELL TRANSPLANTATION
卷 19, 期 12, 页码 1547-1561

出版社

SAGE PUBLICATIONS INC
DOI: 10.3727/096368910X513973

关键词

Cytomegalovirus; Nonhuman primates; Transplantation; Immunosuppression; Infection

资金

  1. Diabetes Research Institute Foundation, Hollywood, FL
  2. National Institute of Health [U19A143900, U19A151728, RO1DK55178]
  3. Juvenile Diabetes Research Foundation International [2004-361, 2004-808]
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [U19AI051728, U19AI043900] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK055178] Funding Source: NIH RePORTER

向作者/读者索取更多资源

This retrospective study reviews the results of our experience with the occurrence of CMV DNAemia in islet cell transplanted cynomolgus monkeys subjected to different immunosuppressive protocols, including induction treatment with thymoglobulin (TMG), with a combination of thymoglobulin and fludarabine (FLUD), with cyclophosphamide, or with daclizumab. CMV DNA in the peripheral blood (CMV DNAemia) of 47 monkeys was quantified by real-time PCR on a weekly to biweekly basis. As compared to other immunosuppressive regimens, and in association with greater decreases in WBC, lymphocyte, CD3(+)CD4(+), and CD3(+)CD8(+) lymphocyte counts, frequent CMV DNAemia occurred earlier (within the first month post-transplant), and was of greater severity and duration in recipients of TMG FLUD. Treatment of recipients with alternative induction agents that resulted in less dramatic reductions in WBC and lymphocyte counts, however, resulted in occurrence of CMV DNAemia after postoperative day 60. The frequency, average intensity, duration, and area under the curve (AUC) for CMV DNAemia in animals receiving TMG FLUD were 75-100%, 4.02 +/- 1.75 copies/ng DNA, 23.0 +/- 5.3 days, and 367.0 +/- 121.1 days x copies/ng DNA, respectively; corresponding values in animals receiving other treatments (0-44%, 0.19 +/- 0.10 copies/ng DNA, 0.5 +/- 0.3 days, and 75.4 +/- 40.2 days x copies/ng DNA, respectively) were significantly different. The value of WBC, T and B cells at the nadir of cell depletion greatly affects the occurrence of CMV DNAemia. No animals developed CMV DNAemia within the next 3 weeks when the lowest value of WBC, lymphocyte, CD3(+), CD3(+)CD4(+), CD3(+)CD8(+), or CD20(+) cells was above 4500, 1800, 300, 200, 150, or 300 cells/mu l, respectively. Oral valganciclovir prophylaxis did not completely prevent the appearance of CMV DNAemia.

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