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KMID : 0366220110460040258
Korean Journal of Hematology
2011 Volume.46 No. 4 p.258 ~ p.264
Clinical implications of chimerism after allogeneic hematopoietic stem cell transplantation in children with non-malignant diseases
Park Mee-Rim

Koh Kyung-Nam
Seo Jong-JIn
Im Ho-Joon
Abstract
Background: The effects of chimerism on outcomes following allogeneic hematopoietic stem cell transplantation (HSCT) are unclear and may differ between diseases. We retrospectively evaluated the association between chimerism and transplant outcomes in children with nonmalignant diseases.

Methods: Chimerism was evaluated using short-tandem repeat polymerase chain reaction (STR-PCR) in 48 patients, with mixed chimerism (MC) defined as greater than 1% recipient cells.

Results: The only variable exerting a significant influence on patients¡¯ chimerism status was the number of infused CD34£« cells. MC was detected in 23 transplants (9 showing transient MC; 10 with sustained low levels [¡Â30%] of autologous cells; and 4 with high-level MC [£¾30%]). The degree of STR-PCR at 28 days after HSCT was significantly higher in patients with high-level MC than those with transient or low-level MC. All patients with transient or low-level MC successfully maintained engraftment and showed a clinical response to HSCT, whereas 2 of the 4 patients with high-level MC experienced graft failure. The incidences of grades II-IV acute and chronic graft-versus-host disease (GVHD) were significantly higher in patients with complete donor chimerism (CC) than MC. We observed no significant survival differences between CC and MC groups. However, the survival rate was lower in patients with high MC than those with low-level or transient MC (P=0.03).

Conclusion: In non-malignant diseases, MC may indicate a tolerant state with a decreased incidence of GVHD. However, high-level MC may signify an increased risk of graft failure and a lower survival rate.
KEYWORD
Non-malignant disease, Allogeneic hematopoietic stem cell transplantation, Chimerism
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