Impact of pretransplant donor-specific anti-HLA antibodies in HLA-mismatched peripheral blood stem cell transplantation

Author:

Hagino Takeshi1ORCID,Ikegame Kazuhiro2ORCID,Tanaka Hidenori3ORCID,Kanda Yoshinobu4ORCID,Kaida Katsuji5,Fukuda Takahiro6,Kondo Yukio7,Sato Maho8,Doki Noriko9ORCID,Nakamae Hirohisa10ORCID,Matsuoka Ken-ichi11ORCID,Mori Yasuo12ORCID,Sano Hideki13ORCID,Eto Tetsuya14,Kawakita Toshiro15,Hashii Yoshiko16,Ichinohe Tatsuo17ORCID,Atsuta Yoshiko18ORCID,Kanda Junya19ORCID

Affiliation:

1. Tama-Hokubu Medical Center, Tokyo Metropolitan

2. Hyogo College of Medicine Hospital

3. HLA Foundation Laboratory

4. Division of Hematology, Department of Medicine, Jichi Medical University, Tochigi, Japan

5. Division of Hematology, Department of Internal Medicine, Hyogo College of Medicine

6. National Cancer Center Hospital

7. Toyama Prefectural Central Hospital

8. Osaka Women’s and Children’s Hospital

9. Tokyo Metropolitan Cancer and Infectious Diseases Center,Komagome Hospital

10. Graduate School of Medicine, Osaka Metropolitan University

11. Okayama University Hospital

12. Kyushu University Hospital

13. Fukushima Medical University Hospital

14. Hamanomachi Hospital

15. Kumamoto Medical Center, National Hospital Organization

16. Osaka University Graduate School of Medicine

17. Research Institute for Radiation Biology and Medicine, Hiroshima University

18. Japanese Data Center for Hematopoietic Cell Transplantation/Nagoya University Graduate School of Medicine

19. Kyoto University

Abstract

Abstract The cut-off levels of donor-specific anti-HLA antibodies (DSAs) that are considered to predict a high risk of graft failure remain unclear. Using peripheral blood stem cell transplantation (PBSCT) data from the Japanese Society for Transplantation and Cellular Therapy/Japanese Data Center for Hematopoietic Cell Transplantation (JSTCT/JDCHCT), we examined the role of DSAs, and performed a retrospective analysis of patients whose recipients underwent related PBSCT between 2010 and 2014 with pre-transplant anti-HLA antibodies. Patients were divided into 3 groups using a mean fluorescence intensity (MFI) of 5,000 as a cut-off value: DSA positive (n = 8), anti-HLA antibody-positive (n = 137) and anti-HLA antibody-negative (n = 3657). There was a significant difference in the number of CD34-positive cells (median: 4.31, 3.97, and 5.33×106/kg, respectively; p < 0.05). Regarding the eight DSA-positive patients, only two underwent therapeutic intervention, and neutrophils were engrafted in all but one patient (median, 10 days). Although there was a statistically significant difference in neutrophil and platelet engraftment among the 3 groups (both p < 0.05), neutrophil engraftment was faster in the DSA group, with no significant difference in the overall survival (p = 0.46). Our results, based on JSTCT/JDCHCT data, suggest that DSAs may not affect the risk in related PBSCT.

Publisher

Research Square Platform LLC

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