TY - JOUR
T1 - Evaluating vaccine-elicited antibody activities against Neisseria gonorrhoeae
T2 - cross-protective responses elicited by the 4CMenB meningococcal vaccine
AU - Gray, Mary C.
AU - Thomas, Keena S.
AU - Lamb, Evan R.
AU - Werner, Lacie M.
AU - Connolly, Kristie L.
AU - Jerse, Ann E.
AU - Criss, Alison K.
N1 - Publisher Copyright:
© 2023 American Society for Microbiology. All rights reserved.
PY - 2023/12
Y1 - 2023/12
N2 - The bacterial pathogen Neisseria gonorrhoeae is an urgent global health problem due to increasing numbers of infections, coupled with rampant antibiotic resistance. Vaccines against gonorrhea are being prioritized to combat drug-resistant N. gonorrhoeae. Meningococcal serogroup B vaccines such as four-component meningococcal B vaccine (4CMenB) are predicted by epidemiology studies to cross-protect individuals from natural infection with N. gonorrhoeae and elicit antibodies that cross-react with N. gonorrhoeae. Evaluation of vaccine candidates for gonorrhea requires a suite of assays for predicting efficacy in vitro and in animal models of infection, including the role of antibodies elicited by immunization. Here, we present the development and optimization of assays to evaluate antibody functionality after immunization of mice: antibody binding to intact N. gonorrhoeae, serum bactericidal activity, and opsonophagocytic killing activity using primary human neutrophils [polymorphonuclear leukocytes (PMNs)]. These assays were developed with purified antibodies against N. gonorrhoeae and used to evaluate serum from mice that were vaccinated with 4CMenB or given alum as a negative control. Results from these assays will help prioritize gonorrhea vaccine candidates for advanced preclinical to early clinical studies and will contribute to identifying correlates and mechanisms of immune protection against N. gonorrhoeae.
AB - The bacterial pathogen Neisseria gonorrhoeae is an urgent global health problem due to increasing numbers of infections, coupled with rampant antibiotic resistance. Vaccines against gonorrhea are being prioritized to combat drug-resistant N. gonorrhoeae. Meningococcal serogroup B vaccines such as four-component meningococcal B vaccine (4CMenB) are predicted by epidemiology studies to cross-protect individuals from natural infection with N. gonorrhoeae and elicit antibodies that cross-react with N. gonorrhoeae. Evaluation of vaccine candidates for gonorrhea requires a suite of assays for predicting efficacy in vitro and in animal models of infection, including the role of antibodies elicited by immunization. Here, we present the development and optimization of assays to evaluate antibody functionality after immunization of mice: antibody binding to intact N. gonorrhoeae, serum bactericidal activity, and opsonophagocytic killing activity using primary human neutrophils [polymorphonuclear leukocytes (PMNs)]. These assays were developed with purified antibodies against N. gonorrhoeae and used to evaluate serum from mice that were vaccinated with 4CMenB or given alum as a negative control. Results from these assays will help prioritize gonorrhea vaccine candidates for advanced preclinical to early clinical studies and will contribute to identifying correlates and mechanisms of immune protection against N. gonorrhoeae.
KW - antibody
KW - complement
KW - imaging flow cytometry
KW - KEYWORDS Neisseria gonorrhoeae
KW - opsonophagocytic killing
KW - serum bactericidal activity
KW - vaccine
UR - http://www.scopus.com/inward/record.url?scp=85180007461&partnerID=8YFLogxK
U2 - 10.1128/iai.00309-23
DO - 10.1128/iai.00309-23
M3 - Article
C2 - 37991382
AN - SCOPUS:85180007461
SN - 0019-9567
VL - 91
JO - Infection and Immunity
JF - Infection and Immunity
IS - 12
ER -