CVID is most frequent symptomatic primary
hypogammaglobulinemia. The foundation of therapy for CVID is
immunoglobulin replacement. The factors that influence the
effect of this therapy are not elucidated. It should be
supposed participation of receptors for immunoglobulins on
professional phagocytes and lymphocytes. We have investigated
41 patients (13 males, 28 females, aged 10-77 years) and 44
age-related control persons. Quantitative expression of the Fc
receptors on the surface of lymphocytes, monocytes, and
granulocytes was determined by flow cytometry. Gene
polymorphism of Fc receptors was determined by PCR. The
expression of CD16, CD 32 and CD64 on lymphocytes and monocytes
was comparable in patients and control persons, also the
expression of CD16 and CD32 on granulocytes was similar in both
groups. However, we have found marked differences in the
expression of CD64 on granulocytes in CVID patients: in
patients with high expression of CD64 on their granulocytes the
clinical state and effectivity of standard treatment with
intravenous immunoglobulin was significantly worse than in
patients with low expression of this receptor. Our results
suggest that the gravity in the clinical course of CVID
patients and efficacy of immunoglobulin therapy may relate to
the upregulation of Fc gamma receptor I (CD64) on granulocytes.