If this is not your name, click here.
| | If this is not your name, click here. | | |
| | Contact Us | Order Now | Journals | Bookstore | Register a colleague | | |
| |  Screening Method Able to Identify Newborns With T-Cell Lymphopenia CHICAGO -- December 8, 2009 -- The testing of DNA from a statewide blood screening program for newborns in Wisconsin was able to identify infants with T-cell lymphopenia, a blood disorder that affects the child’s immune system, a disease in which early identification is important, according to a study in the December 9 issue of JAMA. Infants with severe T-cell lymphopenia, including severe combined immunodeficiency (SCID), often appear normal at birth and have no family history of immunodeficiency. “Consequently, many infants with severe T-cell deficiencies are not identified until life-threatening infections occur,” the authors wrote. “This is an important issue because the long-term prognosis of infants with SCID and other serious immunodeficiencies is markedly improved if the diagnosis is made early, before the onset of serious infections,” They added that the administration of some vaccines that are recommended in early infancy can cause serious infection in infants with T-cell lymphopenia, which could be avoided with early detection. John M. Routes, MD, Medical College of Wisconsin and Children’s Research Institute, Milwaukee, Wisconsin, and colleagues conducted a study to examine if determining the number of T-cell receptor excision circles (TRECs) using DNA extracted from dried blood spots on newborn blood screening (NBS) cards could detect T-cell lymphopenia in newborn infants in a statewide screening program. Between January 1, 2008 and December 31, 2008, the Wisconsin State Laboratory of Hygiene screened all infants born in Wisconsin for T-cell lymphopenia by quantitating the number of TRECs contained in a portion of the NBS card, with the cut-off number being TREC values <25/muL. T-cell lymphopenia was confirmed by further testing. During the study period, 71,000 infants were screened by the TREC assay. Seventeen infants of at least 37 weeks’ gestation had at least 1 abnormal TREC assay, 11 of whom had samples analysed to enumerate T cells. Eight infants demonstrated T-cell lymphopenia, who were then evaluated by a clinical immunologist. The researchers suggest that these results provide support for state screening programs for severe T-cell lymphopenia, with the incidence of primary and secondary immunodeficiencies identified by the TREC assay exceeding the required incidence of disease to institute screening, and the TREC assay being relatively inexpensive. “Based on an analysis of potential cost-effectiveness of NBS for SCID, the relatively high incidence of T-cell lymphopenia and the low cost of the TREC assay suggest NBS may be cost-effective as well, although a formal cost-effectiveness analysis is needed.” “In conclusion, the Wisconsin screening program demonstrates the feasibility of the TREC assay performed on NBS cards to identify infants with primary and secondary forms of T-cell lymphopenia.” SOURCE: JAMA
|
