IC50(μg/ml) for Neut: 2A1-0.00033; 3D5-0.0021; 4G12-0.0020; 5A6-0.0024; 6C7-0.0020; 7B9-0.00027
Target
Alternative Names
HPV; L1; major capsid L1 protein; HPV-16; HPV-16 capsid; HPV16 capsid protein; HPV16 L1; HPV16 major capsid protein L1; Human papillomavirus type 16 L1; Human papillomavirus type 116 major capsid protein L1; Major capsid protein; Major capsid protein L1; Human papillomavirus
Citations
Publication ()
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Background
Papillomaviruses are viruses that cause squamous epithelial and fibroepithelial tumors in their specific host species. In humans, human papillomaviruses (HPVs) can lead to both benign and malignant cell overgrowth, resulting in a wide range of clinical manifestations from genital warts to cervical cancer. HPV infection is the most common sexually transmitted disease, and over 4 types of HPV have been identified to infect the genital tract. Genital HPVs can be categorized as "low-risk" types such as HPV 6 and 11, or "high-risk" types including HPV 16, 18, 31, 33, 35, 39, 45, 52, and 58. The high-risk types are responsible for more than 95% of HPV-induced cervical cancer cases. Preventing cervical cancer through vaccination is considered the most effective approach. Prophylactic HPV vaccines have shown efficacy in clinical trials against HPV infection, cervical intraepithelial neoplasia (CIN), and genital warts. However, these vaccines only target a few specific HPV types. The vaccines are based on papillomavirus-like particles (VLPs) composed of the major capsid protein, L1. VLPs consist of 36 copies of L1 protein arranged into 72 pentamers or capsomeres, forming structures that are immunologically similar to native virions. The VLPs induce a type-specific immune response, with minor cross-neutralization observed mainly between closely related HPV types. Structural analysis has revealed the presence of hypervariable loops on the outer surface of the capsid. Most HPV-neutralizing monoclonal antibodies identified to date are type-specific and recognize conformational epitopes within these surface-exposed hypervariable loops of the L1 protein. This specificity is due to the unique characteristics of each HPV type.
Figure 1. Vaccination against HPV infection using genotype-specific HPV L1 VLPs. (Source: Berzofsky, J. A. et al., 2004)
Anti-HPV 16 L1 monoclonal antibodies are specialized antibodies designed to specifically recognize and bind to the L1 protein of HPV 16. They have significant applications in HPV research, diagnostics, and potentially targeted therapies. These antibodies help researchers understand the biology of HPV and provide potential avenues for developing novel interventions against HPV 16 infection and related diseases.
Alternative Names
Anti-HPV 16 L1 monoclonal antibody Anti-Human Papillomavirus 16 L1 monoclonal antibody Anti-Human papillomavirus type 16 L1 monoclonal antibody Anti-HPV16 major capsid protein L1 monoclonal antibody Anti-Human Papilloma Virus Type 16 major capsid protein L1 monoclonal antibody
References
1. Berzofsky J A, et al. Progress on new vaccine strategies against chronic viral infections. The Journal of Clinical Investigation. 2004, 114(4): 450-462.
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References
Cervarix™: a vaccine for the prevention of HPV 16, 18-associated cervical cancer
Cervical cancer continues to be the second largest cause of cancer deaths in women worldwide. Persistent infection with high-risk types of human papillomavirus (HPV) is a necessary cause of cervical cancer. Thus, prophylactic vaccination against HPV is an attractive strategy to prevent cervical cancer. Current strategies for the development of safe and effective preventive vaccines are based on the induction of neutralizing antibodies against the major capsid protein, L1 of HPV. Cervarix? is one of the preventive HPV vaccines that has been approved in the Europe and Australia and is currently under review by the US Food and Drug Administration. Cervarix is composed of HPV16 and HPV18 L1 virus-like particles (VLPs) formulated in ASO4 adjuvant. Vaccination with Cervarix has been shown to protect women against a high proportion of precursor lesions of cervical cancer caused by these two HPV types. This review explores the various features of this new vaccine candidate and discusses the future directions in the field of HPV vaccine development.
Genital human papillomavirus (HPV) infection with both low- and high-risk types is common, but most infections resolve as a result of a cell-mediated immune response. Failure to induce an effective immune response is related to inefficient activation of innate immunity and ineffective priming of the adaptive immune response; this defective immune response facilitates viral persistence, a key feature of high-risk HPV infection. This milieu becomes operationally HPV antigen tolerant, and the host's defenses become irrevocably compromised. HPV antigen-specific effector cells are poorly recruited to the infected focus and their activity is downregulated; neoplastic HPV containing cervical keratinocytes expressing high levels of E6 and E7 oncoproteins are not killed in this immunosuppressive, tolerant milieu, and progression to high-grade disease and cancer can result. Highly efficacious prophylactic HPV L1 virus-like particle (VLP) vaccines circumvent viral epithelial evasion strategies since they are delivered by intramuscular injection. The stromal dendritic cells of the muscle that encounter the highly immunogenic repeat structure of the VLP then migrate with their cargo to the lymph node, initiating an immune cascade that results in a robust T-cell dependent B-cell response, which generates high levels of L1-specific serum neutralizing antibodies and immune memory.