Immunological reconstitution and correlation of circulating serum inflammatory mediators/cytokines with the incidence of acute graft-versus-host disease during the first 100 days following unrelated umbilical cord blood transplantation

We investigated early immunological reconstitution and the production of circulating inflammatory mediators and their relationship to aGVHD in children during the first 100 days following unrelated UCBT. Nine patients had an underlying malignant disease (ALL, ANLL), and two, non-malignant diseases (SAA, ALD). The median age was 10 years (range: 1.25-21). Seven of 11 patients were alive by day 100, two died from regimen-related toxcity, and two died from severe aGVHD (grade greater than or equal to III). Myeloid engraftment (ANC greater than or equal to 500/mm(3) x 2 days) occurred at a median of 24 days (range: 14-55), while platelet engraftment (platelet count greater than or equal to 20000/mm(3) untransfused x 7 days) was delayed and occurred at a median of 52 days (range: 33-95). The mean cell dose of CD34(+) cells was 3.3+/-3.51 x 10(5)/kg, and of CD34(+)/CD41(+) cells was 3.94+/-3.99 x 10(4)/kg. Acute GVHD (grade II-IV) developed in seven patients (77 %), and severe aGVHD (grade HI-IV) developed in five patients (55%). Serum levels of IL-2R alpha, IL-2, IL-4, IL-7, IL-12, and IFN gamma were not significantly different between patients with grades 0-1 aGVHD and patients with grades II-nr aGVHD. Evaluation of immunological reconstitution on day 90 post UCBT demonstrated an early recovery of the absolute numbers of B cells (CD19(+)) and NK cells (CD3(-)/CD56(+)). Immunoglobulin levels for IgG, IgM and 1gA remained normal throughout the study period. Ph-IN functional studies demonstrated normal superoxide generation, bacterial killing (BK), and chemotaxis (CTX). However, both helper (CD3(+)/CD3(+)) and suppressor (CD3(+)/CD8(+)) T cell subsets remained low during the first 100 days post UCBT with mean +/- s.e.m. values of 120+/-29/mm(3) and 10 +/- 50/mm(3), respectively (normal = 900-2860/mm(3) (CD3/CD4), normal = 630-1910/mm(3) (CD3/CD8)). Mitogen response studies showed low blastogenesis to PHA and PWM, with a mean c.p.m. +/- s.e.m. value of 1.7 +/- 0.67 x 10(4) for PHA (NL greater than or equal to 75 x 10(3)) and 8.42 +/- 4.1 x 10(3) for PWM (NL greater than or equal to 25 x 10(3)). In conclusion, serum levels of inflammatory mediators were not predictive nor did they correlate with the severity of aGVHD. Recovery of NK cells, B cells, and PMN functions occurred within the first 90 days post transplant. However, T cell subsets, CD3(+)/CD4(+) and CD3(+)/CD8(+), and T cell functional activity remained significantly decreased and may account for the high incidence of infectious morbidity seen during this immediate post UCBT period.