Immunotherapeutic Strategies as Potential Treatment Options for Cutaneous Leishmaniasis

被引:6
作者
Lafleur, Andrea [1 ]
Daffis, Stephane [2 ]
Mowbray, Charles [2 ]
Arana, Byron [2 ]
机构
[1] Univ Oxford, Doctoral Training Ctr, Oxford OX1 3NP, England
[2] Drugs Neglected Dis Initiat DNDi, CH-1202 Geneva, Switzerland
基金
英国生物技术与生命科学研究理事会;
关键词
cutaneous leishmaniasis; immunotherapy; TLR agonism; therapeutic vaccination; AZAR DERMAL LEISHMANIASIS; COLONY-STIMULATING FACTOR; PARENTERAL MEGLUMINE ANTIMONIATE; AMPHOTERICIN-B; DOUBLE-BLIND; BALB/C MICE; NEW-WORLD; IN-VITRO; AMAZONENSIS INFECTION; TOPICAL TREATMENT;
D O I
10.3390/vaccines12101179
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cutaneous leishmaniasis (CL), caused by protozoan parasites of the Leishmania genus, is prevalent in tropical and subtropical regions, with important morbidity, particularly in low- to middle-income countries. Current systemic treatments, including pentavalent antimonials and miltefosine, are associated with significant toxicity, reduced efficacy, and are frequently ineffective in cases of severe or chronic CL. Immunotherapies leverage the immune system to combat microbial infection and offer a promising adjunct or alternative approach to the current standard of care for CL. However, the heterogeneous clinical presentation of CL, which is dependent on parasite species and host immunity, may require informed clinical intervention with immunotherapies. This review explores the clinical and immunological characteristics of CL, emphasising the current landscape of immunotherapies in in vivo models and clinical studies. Such immune-based interventions aim to modulate immune responses against Leishmania, with additive therapeutic effects enabling the efficacy of lower drug doses and decreasing the associated toxicity. Understanding the mechanisms that underlie immunotherapy for CL provides critical insights into developing safer and more effective treatments for this neglected tropical disease. Identifying suitable therapeutic candidates and establishing their safety and efficacy are essential steps in this process. However, the feasibility and utility of these treatments in resource-limited settings must also be considered, taking into account factors such as cost of production, temperature stability, and overall patient access.
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页数:41
相关论文
共 246 条
[81]   Recurrent American cutaneous leishmaniasis [J].
Gangneux, Jean-Pierre ;
Sauzet, Sylvie ;
Donnard, Sebastien ;
Meyer, Nicolas ;
Cornillet, Anne ;
Pratlong, Francine ;
Guiguen, Claude .
EMERGING INFECTIOUS DISEASES, 2007, 13 (09) :1436-1438
[82]  
Bustos MFG, 2011, INVEST CLIN, V52, P365
[83]   The development of post-kala-azar dermal leishmaniasis (PKDL) is associated with acquisition of Leishmania reactivity by peripheral blood mononuclear cells (PBMC) [J].
Gasim, S ;
Elhassan, AM ;
Kharazmi, A ;
Khalil, EAG ;
Ismail, A ;
Theander, TG .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2000, 119 (03) :523-529
[84]   Leishmaniasis revisited: Current aspects on epidemiology, diagnosis and treatment [J].
Georgiadou, Sarah P. ;
Makaritsis, Konstantinos P. ;
Dalekos, George N. .
JOURNAL OF TRANSLATIONAL INTERNAL MEDICINE, 2015, 3 (02) :43-50
[85]  
GHALIB HW, 1995, J IMMUNOL, V154, P4623
[86]   Climate Change and Risk of Leishmaniasis in North America: Predictions from Ecological Niche Models of Vector and Reservoir Species [J].
Gonzalez, Camila ;
Wang, Ophelia ;
Strutz, Stavana E. ;
Gonzalez-Salazar, Constantino ;
Sanchez-Cordero, Victor ;
Sarkar, Sahotra .
PLOS NEGLECTED TROPICAL DISEASES, 2010, 4 (01)
[87]   Leishmania donovani inhibits inflammasome-dependent macrophage activation by exploiting the negative regulatory proteins A20 and UCP2 [J].
Gupta, Anand Kumar ;
Ghosh, Kuntal ;
Palit, Shreyasi ;
Barua, Jayita ;
Das, Pijush K. ;
Ukil, Anindita .
FASEB JOURNAL, 2017, 31 (11) :5087-5101
[88]   Interferon-γ treatment induces granulomatous tissue reaction in a case of localized cutaneous leishmaniasis [J].
Haas, N ;
Hauptmann, S ;
Paralikoudi, D ;
Muche, M ;
Kolde, G .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 2002, 24 (04) :319-323
[89]  
Hamidizadeh N, 2017, J PHARM NEGAT RESULT, V8, P43, DOI 10.4103/jpnr.JPNR_1_17
[90]   Therapy of murine cutaneous leishmaniasis by DNA vaccination [J].
Handman, E ;
Noormohammadi, AH ;
Curtis, JM ;
Baldwin, T ;
Sjölander, A .
VACCINE, 2000, 18 (26) :3011-3017