Ab initio calcineurin inhibitor-based monotherapy immunosuppression after liver transplantation reduces the risk for Pneumocystis jirovecii pneumonia

被引:7
|
作者
Orlando, G. [1 ,2 ]
Tariciotti, L. [3 ,4 ]
Manzia, T. M. [3 ,4 ]
Gravante, G. [5 ]
Sorge, R. [6 ]
Manuelli, M. [3 ,4 ]
Pisani, F. [7 ]
Di Cocco, P. [7 ]
Scelzo, C. [8 ]
Burke, G. M. [1 ]
Soker, S. [1 ]
Baiocchi, L. [9 ]
Lerut, J. [10 ]
Angelico, M. [9 ]
Tisone, G. [3 ,4 ]
机构
[1] Wake Forest Inst Regenerat Med, Winston Salem, NC 27157 USA
[2] Univ Oxford, Dept Surg, Oxford, England
[3] Univ Roma Tor Vergata, S Eugenio Hosp, Surg Clin, Rome, Italy
[4] Univ Roma Tor Vergata, S Eugenio Hosp, Transplant Unit, Rome, Italy
[5] Leicester Gen Hosp, Leicester LE5 4PW, Leics, England
[6] Univ Roma Tor Vergata, Dept Human Physiol, Lab Biometry, Rome, Italy
[7] Univ Aquila, San Salvatore Hosp, Transplant & Renal Failure Surg Unit, I-67100 Laquila, Italy
[8] Univ Roma Tor Vergata, Sch Med, Rome, Italy
[9] Univ Roma Tor Vergata, Dept Hepatol, Rome, Italy
[10] Univ Catholique Louvain, Clin St Luc, Serv Chirurg Gen & Transplantat Hepat, B-1200 Brussels, Belgium
关键词
Pneumocystis jirovecii; pneumonia; PCP; prophylaxis; trimethoprim-sulfamethoxazole; monotherapy; liver transplant; immunosuppression; DOSE COTRIMOXAZOLE PROPHYLAXIS; OPERATIONAL TOLERANCE; CARINII-PNEUMONIA; TRIMETHOPRIM-SULFAMETHOXAZOLE; TACROLIMUS MONOTHERAPY; RECIPIENTS; INFECTION; CHEMOPROPHYLAXIS; PREVENTION; SOCIETY;
D O I
10.1111/j.1399-3062.2009.00449.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
At the Tor Vergata University of Rome, ab initio calcineurin inhibitor-based monotherapy immunosuppression (IS) is the standard of treatment after liver transplantation (LT). As the net state of IS determines the onset of Pneumocystis jirovecii pneumonia (PCP), we hypothesized that, in the presence of weak impairment of the immune function, as determined by the above-mentioned IS, the host is not overexposed to the risk for PCP and consequently the specific anti-PCP prophylaxis is unnecessary. In a single-cohort descriptive study, we retrospectively investigated the incidence of PCP in 203 LT patients who did not receive anti-PCP prophylaxis because they were under monotherapy IS. The primary endpoint of the study was the incidence of PCP during the first 12 months following LT; secondary endpoints were the incidence of acute rejection requiring additional IS and of CMV infection. No cases of PCP were recorded. The incidence of CMV and acute rejection was 3.9% and 0.9%, respectively. Our data suggest that monotherapy IS after LT may nullify the risk for PCP even in the absence of any specific prophylaxis.
引用
收藏
页码:11 / 15
页数:5
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