Immune response to the Human Papillomavirus 
      Immune response to  HPV in primary infection;
        Human papillomavirus infection of the cervix is relatively  common in young sexually active women .The majority of infections are transient  and not clinically evident with 70-90% of infections clearing within 12-30 months.  This suggests that host immunity is generally able to clear HPV infection. The  fact that HPV remains localised to cervix and vagina further indicates that  local immune responses are sufficient in controlling and resolving HPV infection.  Both cell mediated immunity and humoral immunity 
        (Antibody responses) have been implicated in the susceptibility,  persistence and clearance of genital HPV infection. 
      Although HPV infection is known to generate an immune  response, it is an elusive target for the immune system and the immune  responses are generally weak.  Several  mechanisms are involved which contribute to immune evasion. 
        1) HPV is non cytopathic i.e.  The viruses do not lyse cells unlike the  herpes viruses for example. They cause cell proliferation rather than cell  destruction and as such do not invoke an inflammatory response  
        2) The fact that HPV only infects epithelial cells  facilitates evasion of the immune system. Complete HPV virions are only found  in terminally differentiating squamous cells in the outer layers of the genital  epithelium, separated by several layers of mucosal epithelium from the lymphocytic  germinal centres in the submucosa which are involved in generating the immune  response
        3) HPV avoids recognition of the innate immune system by  blocking the production of interferons to ensure its own replication. This is  achieved by the production of two early proteins E6 and E7 that bind to and  inactivate intermediates in the interferon cascade.
        Knowledge about the immune response to HPV is important for  the production of appropriate vaccines against the viruses. An ideal HPV  vaccine should induce both antibody and cellular immunity. Studies have shown  that the major capsid protein L1 is essential in this respect. In canine and  rabbit models of HPV infection immunisation with papillomavirus L1 virus like  particles (VLPs) induces neutralising antibodies and totally protects immunised  animals from challenge. There have been two successful clinical trials using  vaccines prepared from VLPs the results of which are discussed in the next  section.
      Strategies for the production of other HPV vaccines using  different production systems can be found in the following publication;
          Strategies for the prevention of cervical cancer by human papillomavirus  vaccination by A-L  Williamson Williamson  . J.-A Passmore and E.P.Rybicki in Best Practice and Research in Clinical  Obstetrics and  Gynaecology2005  vol 19 , no4,   pp 531 - 544 Also available on line at http://www.sciencedirect.com).