
| ID | 32173 |
| JaLCDOI | |
| フルテキストURL | |
| 著者 |
Komatsuda, Mitsumoto
Okayama University
|
| 抄録 | Proportional changes of lymphocyte subsets in the peripheral blood were monitored by two-color flow-cytometry in seven leukemia patients who had received allogenic bone marrow transplantation (BMT). Lymphocyte counts, and proportions of T and B-cells returned to normal ranges between the 2nd and 12th months after BMT. Activated T-cells prominently increased after BMT, and the values gradually returned toward normal. As to lymphocyte subsets, the proportions of CD 4+ cells had remained low, while those of CD 8+ cells high for a whole observation period after BMT. The changes of CD 4+ cells were caused by the decrease of suppressor-inducer T-cells (CD 4+ Leu 8+). High proportion of CD 8+ cells was mainly associated with increased suppressor T-cells (CD 8+ CD 11+). Among natural killer (NK) cells, highly active NK cells (CD 16+ CD 57-) markedly increased shortly after BMT, and gradually returned to normal. CD 16 -CD 57+ NK cells increased beyond normal ranges after the 2nd month. The incidence or degree of acute and chronic graft-versus-host diseases (GVHD) did not correlate with the changes of any lymphocyte subsets. The present results suggest that the increase of activated T-cells shortly after BMT reflects lymphocyte reconstitution. The prolonged immune deficiency after BMT might be related to either deficient expression of homing receptor (Leu 8 antigen) on CD 4+ cells or increased suppressor T-cells (CD 8+ CD 11+). In addition, the early increase of NK cells after BMT may compensate for the immune deficiency in BMT patients. |
| キーワード | immunologic reconstitution
lymphocyte subsets
graft-versus-host diseases
allogenic bone marrow transplantation
|
| Amo Type | Article
|
| 出版物タイトル |
Acta Medica Okayama
|
| 発行日 | 1991-08
|
| 巻 | 45巻
|
| 号 | 4号
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| 出版者 | Okayama University Medical School
|
| 開始ページ | 257
|
| 終了ページ | 265
|
| ISSN | 0386-300X
|
| NCID | AA00508441
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| 資料タイプ |
学術雑誌論文
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| 言語 |
英語
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| 論文のバージョン | publisher
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| 査読 |
有り
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| PubMed ID | |
| Web of Science KeyUT |