Rohan Ameratunga , Danny Lim , Hilary Longhurst , James Mehrtens , Euphemia Leung , Klaus Lehnert , Richard Steele , See-Tarn Woon
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引用次数: 0
Abstract
Aims
This study aimed to establish the reference intervals for the 3H thymidine uptake assays of functional cellular immunity. Functional tests of cellular immunity play a critical role in several clinical scenarios. An excellent T cell response to vaccine antigens is arguably the best in vitro test of normal cellular immunity.
Methods
In this article the reference intervals for over 250 healthy adults were calculated for lectins, anti-CD3 (OKT3) and antigens comprising Candida, tetanus and diphtheria toxoids. These samples were provided by volunteer blood donors as controls to be run in parallel with diagnostic tests of in vitro cellular immunity in patients with suspected immunodeficiency.
Results
The control samples uniformly responded to PHA. The response to other lectins, OKT3 and antigens was more heterogeneous. The variable responses to diphtheria and tetanus toxoids likely reflected the immunization status of these blood donors to these vaccine antigens.
Conclusions
Although there has been a recent move to implement non-radioactive methods for functional cellular immunity, 3H thymidine uptake continues to be utilized in many diagnostic laboratories because of excellent sensitivity. Robust vaccine-induced cellular responses in immunodeficient patients may inform clinical decisions such as using live attenuated viral vaccines. Similarly, markedly impaired responses to phytohemagglutinin A (PHA), in the appropriate clinical context, supports a diagnosis of Severe Combined Immunodeficiency (SCID) and the need for urgent hematopoietic stem cell transplantation (HSCT). The reference intervals established by this audit will assist other diagnostic laboratories using this platform.
期刊介绍:
The Journal of Immunological Methods is devoted to covering techniques for: (1) Quantitating and detecting antibodies and/or antigens. (2) Purifying immunoglobulins, lymphokines and other molecules of the immune system. (3) Isolating antigens and other substances important in immunological processes. (4) Labelling antigens and antibodies. (5) Localizing antigens and/or antibodies in tissues and cells. (6) Detecting, and fractionating immunocompetent cells. (7) Assaying for cellular immunity. (8) Documenting cell-cell interactions. (9) Initiating immunity and unresponsiveness. (10) Transplanting tissues. (11) Studying items closely related to immunity such as complement, reticuloendothelial system and others. (12) Molecular techniques for studying immune cells and their receptors. (13) Imaging of the immune system. (14) Methods for production or their fragments in eukaryotic and prokaryotic cells.
In addition the journal will publish articles on novel methods for analysing the organization, structure and expression of genes for immunologically important molecules such as immunoglobulins, T cell receptors and accessory molecules involved in antigen recognition, processing and presentation. Submitted full length manuscripts should describe new methods of broad applicability to immunology and not simply the application of an established method to a particular substance - although papers describing such applications may be considered for publication as a short Technical Note. Review articles will also be published by the Journal of Immunological Methods. In general these manuscripts are by solicitation however anyone interested in submitting a review can contact the Reviews Editor and provide an outline of the proposed review.