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1.
Trends Parasitol ; 38(10): 904-918, 2022 10.
Article in English | MEDLINE | ID: mdl-35933301

ABSTRACT

Babesiosis is a tick-borne disease caused by intraerythrocytic Babesia parasites. It is a well-known illness in companion animals and livestock, resulting in substantial economic losses in the cattle industry. Babesiosis is also recognized as an emerging zoonosis of humans in many countries worldwide. There is no vaccine against human babesiosis. Currently, preventive measures are focused on vector avoidance. Although not always effective, treatment includes antimicrobial therapy and exchange transfusion. In this review, we discuss the host's immune response to the parasite, vaccines being used to prevent babesiosis in animals, and lessons from malaria vaccine development efforts to inform the development of a human babesiosis vaccine. An effective human vaccine would be a significant advance towards curtailing this rapidly emerging disease.


Subject(s)
Babesia , Babesiosis , Cattle Diseases , Tick-Borne Diseases , Vaccines , Animals , Babesiosis/parasitology , Babesiosis/prevention & control , Cattle , Cattle Diseases/parasitology , Cattle Diseases/prevention & control , Feasibility Studies , Humans
2.
Cell Host Microbe ; 29(6): 894-903.e5, 2021 Jun 09.
Article in English | MEDLINE | ID: mdl-33989514

ABSTRACT

Babesia spp. are tick-transmitted intra-erythrocytic protozoan parasites that infect humans and animals, causing a flu-like illness and hemolytic anemia. There is currently no human vaccine available. People most at risk of severe disease are the elderly, immunosuppressed, and asplenic individuals. B. microti and B. divergens are the predominant species affecting humans. Here, we present a whole-parasite Babesia vaccine. To establish proof-of-principle, we employed chemically attenuated B. microti parasitized red blood cells from infected mice. To aid clinical translation, we produced liposomes containing killed parasite material. Vaccination significantly reduces peak parasitemia following challenge. B cells and anti-parasite antibodies do not significantly contribute to vaccine efficacy. Protection is abrogated by the removal of CD4+ T cells or macrophages prior to challenge. Importantly, splenectomized mice are protected by vaccination. To further facilitate translation, we prepared a culture-based liposomal vaccine and demonstrate that this performs as a universal vaccine inducing immunity against different human Babesia species.


Subject(s)
Babesia microti/immunology , Babesiosis/immunology , Babesiosis/prevention & control , Drug Evaluation, Preclinical , Parasitemia/immunology , Vaccines, Attenuated/immunology , Vaccines, Attenuated/therapeutic use , Animals , Antibodies, Protozoan/blood , B-Lymphocytes/immunology , Babesiosis/parasitology , Drug Delivery Systems/methods , Female , Humans , Immunity , Liposomes/therapeutic use , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Mice, SCID , Parasitemia/therapy , T-Lymphocytopenia, Idiopathic CD4-Positive/immunology , Ticks/parasitology
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