Affiliation:
1. Department of Microbiology and Immunology, Virginia Commonwealth University, Richmond, Virginia
2. Center for the Study of Biological Complexity, Virginia Commonwealth University, Richmond, Virginia
Abstract
ABSTRACT
Cryptosporidiosis is a ubiquitous infectious disease, caused by the protozoan parasites
Cryptosporidium hominis
and
Cryptosporidium parvum
, leading to acute, persistent, and chronic diarrhea with life-threatening consequences in immunocompromised individuals. In developing countries, cryptosporidiosis in early childhood has been associated with subsequent significant impairment in growth, physical fitness, and intellectual abilities. Currently, vaccines are unavailable and chemotherapeutics are toxic and impractical, and agents for immunoprophylaxis or treatment of cryptosporidiosis are a high priority. Availability of the genome sequences for
C. hominis
and
C. parvum
provides new opportunities to procure and examine novel vaccine candidates. Using the novel approach of “reverse vaccinology,” we identified several new potential vaccine candidates. Three of these antigens—Cp15, profilin, and a
Cryptosporidium
apyrase—were delivered in heterologous prime-boost regimens as fusions with cytolysin A (ClyA) in a
Salmonella
live vaccine vector and as purified recombinant antigens, and they were found to induce specific and potent humoral and cellular immune responses, suggesting their potential as new vaccinogens against
Cryptosporidium
infection.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
Cited by
45 articles.
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