Data presented in this study suggest that for TcdB, the latter approach is far from optimal as it omits key toxin-neutralising epitopes. A further important consideration click here in the antigen design is whether the generated antibodies provide protection against a broad range of C. difficile isolates. Antibodies produced with TxA4 potently neutralised TcdA toxinotypes, 0, 3 and 5 with similar efficacy. Potent neutralisation by TxB4 antibodies was also observed against various TcdB toxinotypes albeit with some reduction in neutralising efficacy: <3-fold
against TcdB toxinotypes 3 and 5 and approximately a 7-fold reduction against a TcdB toxinotype 10. It is notable that the latter unusual TcdB Crizotinib molecular weight variant [39] showed least sequence homology compared to TcdB toxinotype 0 (85.7% overall and 88.1% within the central region). In conclusion, the designed constructs TxA4 and TxB4 have several properties which make them attractive as antigen candidates. They can be expressed in a soluble form in scalable, low cost E. coli-based expression systems and were shown to induce the production of antibodies which neutralise
potently key toxinotypes of TcdA and TcdB. In addition, a mixture of the resulting antibodies was shown to afford protection from severe CDI using the hamster infection model. Data presented in the study reveal significant differences between TcdA and TcdB with respect to the domains which evoke a toxin-neutralising immune response. The described antigens will support
large-scale antibody production and so underpin the development of an immunotherapeutic platfom for the treatment of CDI. This report is work commissioned by the National Institute of 3-mercaptopyruvate sulfurtransferase Health Research. The views expressed in this publication are those of the authors and not necessarily those of the NHS, the National Institute for Health Research or the Department of Health. The work reported in this study was funded by the Health Protection Agency, NIHR Centre for Health Protection Research and by the Welsh Development Agency (Smart Award). The authors would also like to thank Kin Chan for his assistance in carrying out the fermentation studies and Dr. Ibrahim Al-Abdulla for his assistance in purifying some of the antibody preparations. Conflict of interest statement: The authors declare that they have no conflict of interest. “
“Cervical cancer (CC) is the third most common cancer in women, with an estimated 530,000 new cases worldwide in 2008 [1]. Despite screening, the burden of CC remains high, with 275,000 deaths estimated for 2008 [1]. The burden of CC varies considerably between countries, with 85% of cases and 88% of deaths occurring in developing nations [1] and [2]. Human papillomavirus (HPV) is established as a necessary cause of CC, with HPV identified in 99.7% of CC cases worldwide [3]. The two HPV types most commonly associated with CC are HPV types 16 and 18.