| Literature DB >> 32231249 |
Sarah Whiteside1, Alex Chin2,3, Gaurav Tripathi2,4, Poonam Dharmani-Khan2,4, Marketa Markova5, Petra Keslova6, Petr Sedlacek6, Michelle N Geddes2,4, Victor Lewis2,4, Monica Modi2, Amit Kalra2, Rosy Dabas2, Ariz Akhter2, Loree Larratt4,7, Tiffany van Slyke4,7, Joseph Brandwein4,7, Stephen R Spellman8, Richard Leigh2,4, Andrew Daly2,4, Faisal M Khan2,3, Jan Storek2,4.
Abstract
Atopy is excessive production of IgE in response to allergens. We evaluated in patients undergoing allogeneic hematopoietic cell transplantation (HCT) the following hypotheses: (1) Atopy is "curable" in atopic patients receiving HCT from a nonatopic donor (D-R+), and (2) Atopy is transferable from atopic donors to nonatopic recipients (D+R-). Atopic patients with atopic donors (D+R+) and non-atopic patients with non-atopic donors (D-R-) served as controls. We measured levels of multiallergen-specific IgE (A-IgE, atopy defined as ≥0.35 kUA/L) in sera from 54 patients and their donors pre HCT and from the patients at ≥2 years post HCT. Only 7/12 (58%) D- R+ patients became nonatopic after HCT. Only 1/11 (9%) D+R- patients became atopic. Eleven of 13 (85%) D-R- patients remained nonatopic. Unexpectedly, 11/18 (61%) D+R+ patients became nonatopic. In conclusion, contrary to our hypothesis and previous reports, the "cure" of atopy may occur in only some D-R+ patients and the transfer of atopy may occur rarely. The "cure" may not be necessarily due to the exchange of atopic for nonatopic immune system, as the "cure" may also occur in D+R+ patients.Entities:
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Year: 2020 PMID: 32231249 DOI: 10.1038/s41409-020-0876-7
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483