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. 2013 Feb;34(1):15–38.

Table 3.

Role of diagnostic/screening tests in immediate and delayed drug hypersensitivity reactions.

In Vivo Ex Vivo

Phenotype SPT/IDT Patch test Oral Challenge (DPT) LTT ELISpot ICS/other ex vivo BAT IgE/RAST HLA Screen
IgE mediated Yes No Yes No No Not routine (specific not sensitive) Yes-screen only (specific not sensitive) No
Delayed Rash (MPE) Yes -delayed IDT reading Yes Possible 5–7 day challenge Yes Yes No No No
DRESS/DIHS Yes - delayed IDT reading Yes No Yes Yes No No Possible
Abacavir HSS No -risk severe reaction Yes No Yes Yes No No Yes HLA-B*5701
SJS/TEN Low sensitivity Low sensitivity No Yes Yes No No Possible
AGEP Yes -delayed IDT reading Yes No Possible Possible No No No
FDE Yes- delayed IDT reading Yes No Possible Limited data No No No
DILI No No No Possible Yes No No Possible

Not routinely used globally in clinical practice as positive predictive value, negative predictive value and number needed to test to prevent one case varies amongst drugs and populations (see Table 4).

Limited data on the performance of LTT on AGEP and FDE. However along with a positive delayed IDT and patch test result as well as a good clinical diagnosis, a positive LTT can help in the identification of the culprit drug. 139 Yet diagnosis should take into account the possibility false positive and negative results, particularly in cases where multiply drugs are under suspicion.

HLA: human leukocyte antigen, LTT: Lymphocyte transformation test, ELISpot: enzyme-linked immunospot, ICS: intracellular cytokine staining, BAT: Basophil Activation Testing, Ig: Immunoglobulin, IDT: intradermal testing, SPT: skin prick testing, HSS: Hypersensitivity syndrome, DRESS: Drug reaction with eosinophilia and systemic symptoms, DIHS: Drug-induced Hypersensitivity syndrome, SJS/TEN: Stevens-Johnson syndrome / Toxic epidermal necrolysis, AGEP: acute generalised exanthematous pustulosis, DILI: Drug-induced liver injury, FDE: Fixed drug eruption.