Leishmaniasis and tumor necrosis factor alpha antagonists in the Mediterranean basin. A switch in clinical expression

被引:32
作者
Bosch-Nicolau, Pau [1 ]
Ubals, Maria [2 ]
Salvador, Fernando [1 ]
Sanchez-Montalva, Adrian [1 ]
Aparicio, Gloria [2 ]
Erra, Alba [3 ]
Martinez de Salazar, Pablo [4 ]
Sulleiro, Elena [4 ]
Molina, Israel [1 ]
机构
[1] Univ Autonoma Barcelona, PROSICS Barcelona, Hosp Univ Vall dHebron, Dept Infect Dis, Barcelona, Spain
[2] Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Dermatol, Barcelona, Spain
[3] Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Rheumatol, Barcelona, Spain
[4] Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Clin Microbiol, PROSICS Barcelona, Barcelona, Spain
关键词
VISCERAL LEISHMANIASIS; CUTANEOUS LEISHMANIASIS; FACTOR THERAPY; PATIENT; INFECTION; INFLIXIMAB; INFANTUM; TNF; HOST; MACROPHAGES;
D O I
10.1371/journal.pntd.0007708
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Tumor necrosis factor alpha (TNF-alpha) blockers are recognized as a risk factor for reactivation of granulomatous infections. Leishmaniasis has been associated with the use of these drugs, although few cases have been reported. Methodology We performed a retrospective observational study including patients with confirmed leishmaniasis acquired in the Mediterranean basin that were under TNF-alpha blockers therapy at the moment of the diagnosis. Patients diagnosed in our hospital from 2008 to 2018 were included. Moreover, a systematic review of the literature was performed and cases fulfilling the inclusion criteria were also included. Principal findings Forty-nine patients were analyzed including nine cases from our series. Twenty-seven (55.1%) cases were male and median age was 55 years. Twenty-five (51%) patients were under infliximab treatment, 20 (40.8%) were receiving adalimumab, 2 (4.1%) etanercept, one (2%) golimumab and one (2%) a non-specified TNF-alpha blocker. Regarding clinical presentation, 28 (57.1%) presented as cutaneous leishmaniasis (CL), 16 (32.6%) as visceral leishmaniasis (VL) and 5 (10.2%) as mucocutaneous leishmaniasis (MCL). All VL and MCL patients were treated with systemic therapies. Among CL patients, 13 (46.4%) were treated with a systemic drug (11 received L-AmB, one intramuscular antimonials and one miltefosine) while 14 (50%) patients were given local treatment (13 received intralesional pentavalent antimonials, and one excisional surgery). TNF-alpha blockers were interrupted in 32 patients (65.3%). After treatment 5 patients (10.2%) relapsed. Four patients with a CL (3 initially treated with local therapy maintaining TNF-alpha blockers and one treated with miltefosine) and one patient with VL treated with L-AmB maintaining TNF-alpha blockers. Conclusions This data supports the assumption that the blockage of TNF-alpha modifies clinical expression of leishmaniasis in endemic population modulating the expression of the disease leading to atypical presentations. According to the cases reported, the best treatment strategy would be a systemic drug and the discontinuation of the TNF-alpha blockers therapy until clinical resolution.
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页数:16
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