Summary and Recommendations from the National Institute of Allergy and Infectious Diseases (NIAID) Workshop “Gonorrhea Vaccines: the Way Forward”
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C. Deal | P. Rice | I. Feavers | S. Gray-Owen | A. Jerse | L. Wetzler
[1] S. Gray-Owen,et al. The reproductive cycle is a pathogenic determinant during gonococcal pelvic inflammatory disease in mice , 2015, Mucosal Immunology.
[2] Marleen Temmerman,et al. Global Estimates of the Prevalence and Incidence of Four Curable Sexually Transmitted Infections in 2012 Based on Systematic Review and Global Reporting , 2015, PloS one.
[3] Richard T. Gray,et al. The potential impact of vaccination on the prevalence of gonorrhea , 2015, Vaccine.
[4] David M. Curran,et al. Nonbinding Site-Directed Mutants of Transferrin Binding Protein B Exhibit Enhanced Immunogenicity and Protective Capabilities , 2014, Infection and Immunity.
[5] H. Rees,et al. Vaccines against sexually transmitted infections: the way forward. , 2014, Vaccine.
[6] M. Temmerman,et al. Special issue Sexually transmitted infections: vaccine development for global health: preface , 2014 .
[7] M. Russell,et al. Enhancement of adaptive immunity to Neisseria gonorrhoeae by local intravaginal administration of microencapsulated interleukin 12. , 2013, The Journal of infectious diseases.
[8] S. Ram,et al. Immunization against a Saccharide Epitope Accelerates Clearance of Experimental Gonococcal Infection , 2013, PLoS pathogens.
[9] S. Ram,et al. Does Binding of Complement Factor H to the Meningococcal Vaccine Antigen, Factor H Binding Protein, Decrease Protective Serum Antibody Responses? , 2013, Clinical and Vaccine Immunology.
[10] Matthew Hickman,et al. Introducing vaccination against serogroup B meningococcal disease: An economic and mathematical modelling study of potential impact , 2013, Vaccine.
[11] M. Jit,et al. Comparing bivalent and quadrivalent human papillomavirus vaccines: economic evaluation based on transmission model , 2011, BMJ : British Medical Journal.
[12] W. Shafer,et al. Experimental Gonococcal Infection in Male Volunteers: Cumulative Experience with Neisseria gonorrhoeae Strains FA1090 and MS11mkC , 2011, Front. Microbio..
[13] Hong Wu,et al. Estradiol-Treated Female Mice as Surrogate Hosts for Neisseria gonorrhoeae Genital Tract Infections , 2011, Front. Microbio..
[14] A. Jerse,et al. Vaccines for Gonorrhea: Can We Rise to the Challenge? , 2011, Front. Microbio..
[15] M. Russell,et al. New Concepts in Immunity to Neisseria Gonorrhoeae: Innate Responses and Suppression of Adaptive Immunity Favor the Pathogen, Not the Host , 2011, Front. Microbio..
[16] Sue J Goldie,et al. Health and economic implications of HPV vaccination in the United States. , 2008, The New England journal of medicine.
[17] M. Apicella,et al. The Molecular Mechanisms Used by Neisseria gonorrhoeae To Initiate Infection Differ between Men and Women , 2004, Clinical Microbiology Reviews.
[18] D. Granoff,et al. Meningococcal conjugate vaccine for Africa: a model for development of new vaccines for the poorest countries , 2003, The Lancet.
[19] C. Deal,et al. Experimental Gonococcal Urethritis and Reinfection with Homologous Gonococci in Male Volunteers , 2001, Sexually transmitted diseases.
[20] A. Jerse,et al. Intranasal immunization with gonococcal outer membrane preparations reduces the duration of vaginal colonization of mice by Neisseria gonorrhoeae. , 2000, The Journal of infectious diseases.
[21] Myron S. Cohen,et al. A Neisseria gonorrhoeae Immunoglobulin A1 Protease Mutant Is Infectious in the Human Challenge Model of Urethral Infection , 1999, Infection and Immunity.
[22] M. Hobbs,et al. The transferrin receptor expressed by gonococcal strain FA1090 is required for the experimental infection of human male volunteers , 1998, Molecular microbiology.
[23] S. Gulati,et al. Immunogenicity of Neisseria gonorrhoeae lipooligosaccharide epitope 2C7, widely expressed in vivo with no immunochemical similarity to human glycosphingolipids. , 1996, The Journal of infectious diseases.
[24] A. Cross,et al. Experimental human gonococcal urethritis: 250 Neisseria gonorrhoeae MS11mkC are infective. , 1995, The Journal of infectious diseases.
[25] A. Cross,et al. Inflammatory cytokines produced in response to experimental human gonorrhea. , 1995, The Journal of infectious diseases.
[26] N. Nagelkerke,et al. Antibodies to opacity proteins (Opa) correlate with a reduced risk of gonococcal salpingitis. , 1994, The Journal of clinical investigation.
[27] J. Cannon,et al. Human experimentation with Neisseria gonorrhoeae: rationale, methods, and implications for the biology of infection and vaccine development. , 1994, The Journal of infectious diseases.
[28] R. Brunham,et al. Antibody to Rmp (outer membrane protein 3) increases susceptibility to gonococcal infection. , 1993, Journal of Clinical Investigation.
[29] J. Sadoff,et al. Efficacy trial of a parenteral gonococcal pilus vaccine in men. , 1991, Vaccine.
[30] L Slaney,et al. Epidemiologic evidence for the development of serovar-specific immunity after gonococcal infection. , 1989, The Journal of clinical investigation.
[31] E. Tramont. Gonococcal vaccines , 1989, Clinical Microbiology Reviews.
[32] C. P. Kenny,et al. Gonococcal vaccine studies in Inuvik. , 1974, Canadian journal of public health = Revue canadienne de sante publique.
[33] In Men with , 2004 .