The High Dose Therapy of Anti-Human Lymphoblast Globulin in Living Related Renal Transplantation

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Title ( eng )
The High Dose Therapy of Anti-Human Lymphoblast Globulin in Living Related Renal Transplantation
Title ( jpn )
生体腎移植における抗リンパ芽球グロブリン大量療法
Creator
Dohi Kiyohiko
Fukuda Yasuhiko
Asahara Toshimasa
Yahata Hiroshi
Ono Eiji
Takenaka Masaharu
Marubayashi Seiji
Omotehara Tamon
Tabe Yasuji
Eto Takaaki
Ezaki Haruo
Source Title
Hiroshima Journal of Medical Sciences
Volume 33
Issue 2
Start Page 223
End Page 231
Journal Identifire
[PISSN] 0018-2052
[EISSN] 2433-7668
[NCID] AA00664312
Abstract
Large doses of antihuman lymphoblast globulin (AHLG) were used prophylactically in three recipients of renal allografts from living related donors. These recipients received 1,500 mg/day of AHLG for 14 days beginning on the second day before transplantation in addition to the standard immunosuppression. Serum AHLG levels, serum anti-AHLG antibodies and T cell subsets were checked serially. The results were as follows:

1) No side effects and or complications of AHLG were encountered in these recipients.
2) None of patients treated with AHLG had any rejection episodes within three months after transplantation but after that several rejections occurred in two patients.
3) Maximum serum AHLG concentrations, reached at 10-12 days after transplantation, ranged from 252 mg/dl to 465 mg/dl. Serum AHLG levels were detected at least one month after final injection of AHLG.
4) No patients made detectable antibodies to horse IgG.
5) The values of T cell counts, % T cell and T cell subsets (Leu 3a/2a) varied considerable from patient to patient, in two cases were kept moderately low by AHLG treatment. We concluded that the effect of AHLG on T cell subsets was not distinctive.
Keywords
AHLG
Lymphocyte subpopulation
Kidney transplantation
NDC
Medical sciences [ 490 ]
Language
eng
Resource Type departmental bulletin paper
Publisher
Hiroshima University School of Medicine
Date of Issued 1984-06
Publish Type Version of Record
Access Rights open access
Source Identifier
[ISSN] 0018-2052
[NCID] AA00664312
[PMID] 6384144