Dd. Stapleton et al., INDUCTION IMMUNOSUPPRESSION WITH THE MONOCLONAL-ANTIBODY OKT3 AFTER CARDIAC TRANSPLANTATION, The American journal of the medical sciences, 306(1), 1993, pp. 16-19
The routine use of monoclonal induction immunosuppression with OKT3 af
ter orthotopic heart transplantation remains controversial. This study
examined the clinical response of prophylactic monoclonal induction i
mmunosuppression versus standard triple-drug immunosuppression in 41 p
atients who underwent orthotopic heart transplantation from January 19
89 to December 1990 at this institution. Of these, eight received mono
clonal induction immunosuppression for a period of 10 to 14 days. All
patients received identical triple-drug immunosuppression with the exc
eption of cyclosporine starting on the fifth postoperative day in thos
e who received OKT3. At 6 months the duration of hospitalization, free
dom from rejection, incidence of infection requiring hospitalization,
and serum creatinine in the monoclonal induction immunosuppression and
triple-drug groups were compared. It was found that the length of hos
pital stay in the OKT3 group was 14.3 +/- 4.5 days, compared with 14.7
+/- 4.7 days in the triple-drug group and that freedom from rejection
was 66% in the OKT3 group compared with 75% in the triple-drug group.
In addition, it was found that the incidence of infection was 36% in
the OKT3 group compared with 38% in the triple-drug group and that ser
um creatinine at 6 months was 1.36 +/- 0.26 mg/dl in the OKT3 group co
mpared with 1.45 +/- 0.73 mg/dl in the triple-drug group. Finally, pat
ient survival at 1 year for the monoclonal induction immunosuppression
group was 100% compared with 91% for the triple-drug group. It was co
ncluded that induction immunosuppression with monoclonal induction imm
unosuppression does not reduce the duration of hospitalization or the
incidence of rejection, change the incidence of infection, alter renal
function, decrease the incidence of allograft coronary artery disease
, or improve the survival rate as compared with standard triple-drug i
mmunosuppression.