Goto Norihiko, Takahashi-Nakazato Ai, Futamura Kenta, Okada Manabu, Yamamoto Takayuki, Tsujita Makoto, Hiramitsu Takahisa, Narumi Shunji, Tsuchiya Kiyoto, Gatanaga Hiroyuki, Watarai Yoshihiko, Oka Shinichi
Department of Transplant Surgery, Japanese Red Cross Nagoya Daini Hospital, Nagoya, Japan.
AIDS Clinical Center, National Center for Global Health and Medicine, Tokyo, Japan.
Transplant Direct. 2017 Apr 5;3(5):e151. doi: 10.1097/TXD.0000000000000665. eCollection 2017 May.
Outbreaks of pneumonia (PCP) in kidney transplant recipients are frequently reported worldwide. However, the general guidelines propose only short-term prophylaxis with trimethoprim-sulfamethoxazole after kidney transplantation. We experienced 3 PCP outbreaks in the last 10 years despite providing the recommended prophylaxis. The purpose of this study was to find a prophylaxis regimen that could successfully prevent future PCP outbreaks in immunosuppressed kidney transplant recipients.
Occurrence of PCP at our hospital since 2004 was reviewed. A total of 48 cases were diagnosed from July 2004 through December 2014. Genotypes of were determined in these cases.
Three PCP outbreaks by 3 different genotypes of in each outbreak occurred with 2-year intervals in last 10 years. Molecular analysis showed that each intraoutbreak was caused by identical , whereas interoutbreaks were caused by different genotypes. Although short-term prophylaxis was provided to all kidney recipients after each outbreak after identification of a single PCP case, additional outbreaks were not prevented because the universal prophylaxis had already been completed when new case of PCP emerged.
The contagious nature of allows easy development of outbreaks of PCP in immunosuppressed kidney transplant recipients. Although the universal short-term prophylaxis is effective in controlling ongoing outbreak, lifelong prophylaxis of kidney transplant recipients should be considered to prevent new outbreaks.
肾移植受者中卡氏肺孢子虫肺炎(PCP)的暴发在全球范围内屡有报道。然而,一般指南仅建议在肾移植后进行短期的甲氧苄啶-磺胺甲恶唑预防。尽管我们按照推荐进行了预防,但在过去10年中仍经历了3次PCP暴发。本研究的目的是找到一种预防方案,能够成功预防免疫抑制的肾移植受者未来发生PCP暴发。
回顾了我院自2004年以来PCP的发生情况。2004年7月至2014年12月共诊断出48例病例。对这些病例进行了卡氏肺孢子虫的基因型测定。
在过去10年中,3种不同基因型的卡氏肺孢子虫分别引发了3次PCP暴发,暴发间隔为2年。分子分析表明,每次暴发内均由相同的卡氏肺孢子虫引起,而不同次暴发由不同基因型引起。尽管在每次暴发中确诊首例PCP病例后,对所有肾移植受者都进行了短期预防,但新的PCP病例出现时,由于已经完成了普遍预防,所以未能预防额外的暴发。
卡氏肺孢子虫的传染性使得免疫抑制的肾移植受者容易发生PCP暴发。尽管普遍的短期预防在控制正在进行的暴发方面有效,但应考虑对肾移植受者进行终身预防以防止新的暴发。