Mh. Yamani et al., Hypogammaglobulinemia following cardiac transplantation: A link between rejection and infection, J HEART LUN, 20(4), 2001, pp. 425-430
Background: Hypogammaglobulinemia (HGG) has been reported after solid organ
transplantation and is noted to confer an increased risk of opportunistic
infections.
Objectives: In this study, we sought to assess the relationship between sev
ere HGG to infection and acute cellular rejection following heart transplan
tation.
Methods: Between February 1997 and January 1999, we retrospectively analyze
d the clinical outcome of 111 consecutive heart transplant recipients who h
ad immunoglobulin G (IE;G) level monitoring at 3 and 6 months post-transpla
nt and when clinically indicated.
Results: Eighty-one percent of patients were males, mean age 54 +/-: 13 yea
rs, and the mean follow-up period was 13.8 +/- 5.7 months. Patients had nor
mal IgG levels prior to transplant (mean 1137 +/- 353 mg/dl). Ten percent (
11 of 111) of patients developed severe HGG (IgG < 350 mg/dl) post-transpla
nt. The average time to the lowest IgG level was 196 <plus/minus> 125 days.
Patients with severe HGG were at increased risk of opportunistic infection
s compared to patients with IgG > 350 mg/dl (55% [6 of 11] vs 5% [5 of 100]
, odds ratio = 22.8, p < 0.001). Compared to patients with no rejection, pa
tients who experienced three or more episodes of rejection had lower mean I
gG (580 <plus/minus> 309 vs 751 +/- 325, p = 0.05), and increased incidence
of severe HGG (33% [7 of 21] vs 2.8% [1 of 35], p = 0.001). The incidence
of rejection episodes per patient at 1 year was higher in patients with sev
ere HGG compared to patients with IgG >350 (2.82 +/- 1.66 vs 1.36 +/- 1.45
episodes/patient, p = 0.02). The use of parenteral steroid pulse therapy wa
s associated with an increased risk of severe HGG (odds ratio = 15.28, p <
0.001).
Conclusions: Severe HGG after cardiac transplantation may develop as a cons
equence of intensification of immunosuppressive therapy for rejection and h
ence, confers an increased risk of opportunistic infections. IgG level may
be a useful marker for identifying patients at high risk.