Estimation of the Minimal Rift Valley Fever Virus Protective Neutralizing Antibody Titer in Human Volunteers Immunized with MP-12 Vaccine Based on Protection in a Mouse Model of Disease

Author:

Watts Douglas M.1,Westover Jonna L.B.2,Palermo Pedro M.1,Bailey Kevin W.2,Morrill John C.3,Bettinger George E.1,Monath Thomas P.4,Smith Darci R.5,Peters Clarence J.6,Pittman Phillip R.7,Orbegozo Jeanette1,Gowen Brian B.2

Affiliation:

1. Department of Biological Sciences and Border Biomedical Research Center, The University of Texas at El Paso, University of Texas at El Paso, El Paso, Texas;

2. Institute for Antiviral Research and Department of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan, Utah;

3. Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Texas;

4. Crozet BioPharma LLC, Devens, Massachusetts;

5. Department of Microbiology and Immunology, Naval Medical Research Center, Biological Defense Research Directorate, Fort Detrick, Maryland;

6. Department of Pathology and Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Texas;

7. Department of Clinical Research 2 U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID), Frederick, Maryland

Abstract

ABSTRACT. The Rift Valley fever virus (RVFV) MP-12 vaccine is a promising human and veterinary vaccine. Although the vaccine elicited neutralizing antibody (nAb) in human volunteers, the minimal antibody titer that is needed to afford protection is unknown. Therefore, this study was conducted to determine the minimal nAb titer elicited by the RVFV MP-12 vaccine in human volunteers that protected mice against lethal RVFV challenge as a surrogate assessment of the protective efficacy of the vaccine. Among volunteers who were vaccinated with the MP-12 vaccine during a phase II trial, sera with antibody titers of 1:20 collected 5 years post-vaccination (PV), 1:40 titer collected 2 years PV, and 1:80 titer collected 1 year PV was passively transferred to groups of BALB/c mice. Blood samples were obtained 1 day after passive transfer to determine the RVFV neutralizing nAb titer before challenge with pathogenic RVFV (strain ZH501). Our results indicated that 1 day after passive transfer of the immune sera, an approximate 4-fold reduction in circulating nAb titers was detected in the mice. The presence of RVFV nAb titers in the range of 1:5 to 1:20 were generally protective (75–100% survival). These results suggested that circulating titers of 1:5 or higher offer a high degree of protection by MP-12-elicited antibody in human volunteers. Also, the findings highlighted the value of using the BALB/c mouse RVFV challenge model as a surrogate for evaluating the protective nAb responses elicited by MP-12 and possible use for evaluating the efficacy of other RVFV vaccine candidates.

Publisher

American Society of Tropical Medicine and Hygiene

Subject

Virology,Infectious Diseases,Parasitology

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