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ShareDec. 10, 2008 — A study published by Elsevier this month in Clinical Immunology, the official journal of the Clinical Immunology Society (CIS), describes a new method that facilitates the induction of a specific type of immune suppressive cells, called ‘regulatory T cells’ for therapeutic use. These immune suppressive cells show great potential for the treatment of autoimmune diseases and improving transplantation outcomes.
Immunotherapy refers to a collection of treatments based upon the concept of modulating the immune system to achieve a prophylactic and/or therapeutic goal. For example, inducing immune suppression could dampen an abnormal immune response in autoimmune diseases or could reduce a normal immune response to prevent rejection of transplanted organs or cells. Regulatory T cells are an important part of the immune system and can play a suppressive role, but naturally occur in low numbers.
Michael Albert and colleagues from the Ludwig-Maximilians-University in Munich, Germany, describe a unique strategy that facilitates the induction of regulatory T cells ex vivo with subsequent expansion to numbers adequate for immunotherapy. Using an inexpensive, fast and simple high-yield method they generated regulatory T cells from small amounts of peripheral blood which, potentially, could be transferred back into a patient enabling a clinically desired immune suppression.
“Feasible protocols to provide large amounts of regulatory T cells are in great demand”, said Andy Saxon”, the Editor-in-Chief of Clinical Immunology, “this article describes a relative simple but exciting method which can be used in clinical settings such as transplantation”.
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The above story is reprinted from materials provided by Elsevier, via AlphaGalileo.
Note: Materials may be edited for content and length. For further information, please contact the source cited above.
Journal Reference:
- Michael H. Albert, Xue-Zhong Yu and Thomas Magg. Ethylenecarbodiimide-coupled allogeneic antigen presenting cells induce human CD4 regulatory T cells. , 2008; 129 (3): 381-393 DOI: 10.1016/j.clim.2008.07.027
Note: If no author is given, the source is cited instead.
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