TY - JOUR KW - Cytokines KW - Etanercept KW - Humans KW - Immunoglobulin G KW - Immunoglobulins, Intravenous KW - Immunologic Factors KW - Immunosuppressive Agents KW - Immunotherapy KW - Interferon-gamma KW - Interleukin-2 KW - Mycobacterium tuberculosis KW - Prednisolone KW - Receptors, Tumor Necrosis Factor KW - Th1 Cells KW - Th2 Cells KW - Thalidomide KW - Tuberculosis Vaccines KW - Tuberculosis, Pulmonary AU - Guo S AU - Zhao J AB -

A Th1/Th2 imbalance in tuberculosis (TB) patients caused by a decreased Th1 response and an increased Th2 response is a significant factor in the pathogenesis and development of TB. Protective immune responses to TB include bacteriostatic and bactericidal responses. Unfortunately, however, immunoprotection and immune pathology co-exist in TB patients. Immunotherapy for TB principally aims to restore the Th1/Th2 balance by enhancing the Th1 response and suppressing the excessive Th2 response. Immunotherapy for TB can be classified into three categories: immune-enhancing therapy using cytokines, immunosuppressive therapy, and immunomodulatory therapy. Immunomodulatory therapy targets the Th1/Th2 imbalance and includes cytokine regulation therapy, antibody regulation therapy, a multi-dose heat-inactivated Mycobacterium vaccae vaccine, thymosin hormones and a DNA vaccine. A new approach in supplementary TB immunotherapy is to simultaneously up-regulate the Th1 response and down-regulate the Th2 response. While immunotherapy can contribute to TB treatment, it may also cause immunopathological injury. Therefore, immunotherapy needs to be improved and further studied to maximize its potential.

BT - Frontiers in bioscience (Landmark edition) C1 - http://www.ncbi.nlm.nih.gov/pubmed/22652806?dopt=Abstract DA - 2012 Jun 01 DO - 10.2741/4079 J2 - Front Biosci (Landmark Ed) LA - eng N2 -

A Th1/Th2 imbalance in tuberculosis (TB) patients caused by a decreased Th1 response and an increased Th2 response is a significant factor in the pathogenesis and development of TB. Protective immune responses to TB include bacteriostatic and bactericidal responses. Unfortunately, however, immunoprotection and immune pathology co-exist in TB patients. Immunotherapy for TB principally aims to restore the Th1/Th2 balance by enhancing the Th1 response and suppressing the excessive Th2 response. Immunotherapy for TB can be classified into three categories: immune-enhancing therapy using cytokines, immunosuppressive therapy, and immunomodulatory therapy. Immunomodulatory therapy targets the Th1/Th2 imbalance and includes cytokine regulation therapy, antibody regulation therapy, a multi-dose heat-inactivated Mycobacterium vaccae vaccine, thymosin hormones and a DNA vaccine. A new approach in supplementary TB immunotherapy is to simultaneously up-regulate the Th1 response and down-regulate the Th2 response. While immunotherapy can contribute to TB treatment, it may also cause immunopathological injury. Therefore, immunotherapy needs to be improved and further studied to maximize its potential.

PY - 2012 SP - 2684 EP - 90 T2 - Frontiers in bioscience (Landmark edition) TI - Immunotherapy for tuberculosis: what's the better choice? VL - 17 SN - 1093-4715 ER -