Skip to main content
. Author manuscript; available in PMC: 2022 Jan 11.
Published in final edited form as: J Allergy Clin Immunol. 2021 May 24;149(1):410–421.e7. doi: 10.1016/j.jaci.2021.04.036

TABLE VI.

Outcomes of engrafted survivors

Outcome Patients (n = 48)
Alive and well with phenotype reversal 41 (85)
 Full donor chimerism (>95%)* 33 (69)
 Mixed CD3+ donor chimerism only (<95%) 3 (6)
 Mixed donor chimerism in both compartments (<95%) 3 (6)
 Other§ 2 (6)
Alive with phenotype reversal but significant ongoing complications|| 4 (8)
Other 3 (6)
 Partial phenotype reversal, mixed donor chimerism 2 (4)
 Too early to evaluate phenotype reversal (<100 days post-HCT) 1 (2)

Values are n (%).

*

Whole blood or myeloid donor chimerism >95%; CD3+ chimerism, if available (n = 14), was >95%.

Whole blood or myeloid donor chimerism >95%; CD3+ chimerism <95% (9.2%, 40%, 93%).

Whole blood or myeloid donor chimerism <95% (range, 52%−82%) and CD3+ himerism <95% (range, 67.5%−84%).

§

Whole blood donor chimerism <95% (n = 1, 94%) and full CD3+ donor chimerism but mixed myeloid and whole blood donor chimerism (n = 1, 96%, 86%, 90%, respectively).

||

Ongoing complications include GVHD (n = 2) and chronic kidney disease (n = 2). All have 100% donor chimerism.

One patient has resolution of recurrent respiratory infections and enteropathy with negative EBV, CMV, and adenovirus in blood, but recent ocular HSV and VZV despite prophylaxis 2 years post-HCT; last donor chimerism: 35% whole blood, 26% myeloid, 34% CD3+, 17% CD19+. The other patient has improvement of disseminated Mycoplasma orale infection but continued immune thrombocytopenia and hypogammaglobulinemia 2.8 years post-HCT; last donor chimerism: 85% myeloid, 58% CD3+, 99% CD19+, 82% natural killer.