Advancing knowledge of the immunological mechanisms of action of existing vaccines provides essential

information that is vital to the production of new, well-tolerated, effective vaccines. How immunological requirements are balanced with the complexities of the pathogen, the needs of the target vaccinees, the practicalities of antigen production, and the stability and tolerability of the eventual vaccine represents a constantly evolving challenge. The factors affecting the selection and production of different types of antigens are discussed in Chapter 3 – Vaccine antigens. “
“Key concepts ■ Many vaccines are comprised of whole viruses or bacteria and therefore contain www.selleckchem.com/products/Trichostatin-A.html many, often poorly defined, antigens as well as other microbial molecules important in triggering innate and/or adaptive immune responses Vaccine antigens include whole live pathogens (modified to reduce their virulence), individual pathogen components (eg protein or polysaccharides) and the genetic material of the pathogen (ie ‘naked’ DNA/RNA) which can direct the production of the vaccine antigen in the recipient. The earliest

vaccine consisted of infected fluid derived from people infected with cowpox, which was used by Edward Jenner to prevent the significantly more serious human disease of smallpox. What Jenner did not know was that the infected fluid used contained live cowpox virus. Cowpox virus shares antigenic components with smallpox, but is much less virulent or pathogenic in humans. Consequently, vaccinees developed CX-5461 research buy immunity to smallpox without the risk of serious disease. Subsequent empirical observations in the 19th century noted that pathogens with reduced virulence and even dead pathogenic bacteria also acted as vaccines. This breakthrough allowed the development of attenuated and inactivated whole-pathogen vaccines, pioneered by the work of Louis Pasteur and Robert Koch. A paradigm shift occurred in the late 19th and early 20th centuries new as a result of progress in biochemistry and the development of vaccines based on toxins, or their inactivated derivatives, the toxoids ( Figure 3.1). The realisation

that the whole pathogen was not always needed to induce immunity, and the subsequent concept of ‘antigen’, were essential to improvements in the safety and efficacy of prophylactic vaccines. It is important to note that most vaccines in this period were successfully developed in the absence of a solid understanding of the immunological responses induced by vaccines or key physical structures of the targeted pathogens. Today, a better understanding of host–pathogen interactions and of the key features needed to induce a proper immune response allows for a more scientific (rational, hypothesis-based approach), rather than empirical (trial and error), approach to the choice and definition of the target antigen(s). In the late 19th and early 20th centuries, bacterial constituents were defined as ‘antigen’, and later as ‘immunogen’.