High-dose polyclonal intravenous immunoglobulin therapy for refractory viral infections including viremia after allogeneic hematopoietic cell transplantation
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- IDO Kentaro
- Hematology, Graduate School of Medicine, Osaka City University
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- NAKANE Takahiko
- Hematology, Graduate School of Medicine, Osaka City University
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- OKAMURA Hiroshi
- Hematology, Graduate School of Medicine, Osaka City University
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- NANNO Satoru
- Hematology, Graduate School of Medicine, Osaka City University
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- NISHIMOTO Mitsutaka
- Hematology, Graduate School of Medicine, Osaka City University
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- HIROSE Asao
- Hematology, Graduate School of Medicine, Osaka City University
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- NAKAMAE Mika
- Hematology, Graduate School of Medicine, Osaka City University
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- NAKASHIMA Yasuhiro
- Hematology, Graduate School of Medicine, Osaka City University
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- KOH Hideo
- Hematology, Graduate School of Medicine, Osaka City University
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- HINO Masayuki
- Hematology, Graduate School of Medicine, Osaka City University
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- NAKAMAE Hirohisa
- Hematology, Graduate School of Medicine, Osaka City University
Bibliographic Information
- Other Title
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- 同種造血細胞移植後難治性ウイルス血症・感染症に対する高用量polyclonal intravenous immunoglobulin
- 臨床研究 同種造血細胞移植後難治性ウイルス血症・感染症に対する高用量polyclonal intravenous immunoglobulin
- リンショウ ケンキュウ ドウシュ ゾウケツ サイボウ イショク ゴ ナンチセイ ウイルス ケッショウ ・ カンセンショウ ニ タイスル コウヨウリョウ polyclonal intravenous immunoglobulin
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Abstract
<p>Refractory viremia/viral disease is a major life-threatening complication that may arise among patients undergoing allogeneic hematopoietic cell transplantation (allo-HCT). This study aimed to clarify the therapeutic effect of high-dose polyclonal intravenous immunoglobulin (IVIG) against viremia/viral diseases after allo-HCT. We conducted a pilot study to investigate the therapeutic effect of 400 mg/kg of IVIG given for 5 consecutive days against refractory viremia/viral disease after allo-HCT. Overall, 7 patients were drug-resistant and the other 7 had not previously received any drug for their viremia/viral disease. All patients completed the 5-day therapy regimen of IVIG. A complete response at Day 56 was observed for 8 of 14 patients (57.1%). Additionally, 10 of 14 patients (71.4%) were alive at Day 56, although only one death occurred due to the viremia/viral disease. Remarkably, all 3 cases who developed exogenous viremia/viral diseases including respiratory syncytial virus pneumonia/bronchitis and human parvovirus B19 viremia achieved a complete response, suggesting that high-dose polyclonal IVIG may be more effective against exogenous viruses rather than endogenous ones. Congestive heart failure was observed in 1 patient. High-dose polyclonal IVIG could be an effective and feasible therapy for refractory viremia/viral disease after allo-HCT.</p>
Journal
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- Rinsho Ketsueki
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Rinsho Ketsueki 61 (3), 215-222, 2020
The Japanese Society of Hematology
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Keywords
Details 詳細情報について
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- CRID
- 1390846609819048192
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- NII Article ID
- 130007821384
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- NII Book ID
- AN00252940
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- ISSN
- 18820824
- 04851439
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- NDL BIB ID
- 030383323
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- PubMed
- 32224580
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed