We investigated peripheral lymphocyte subsets in 34 consecutive acute
pancreatitis patients (21 males, 13 females; mean age, 57 years; range
, 16-85 years) studied within 48 h of pain onset and for 5 consecutive
days to understand better the immunological response during the cours
e of the disease. The diagnosis was based on characteristic abdominal
pain associated with a twofold increase in serum lipase and confirmed
by imaging techniques in all patients. Acute pancreatitis was of bilia
ry origin in 25 patients, due to alcohol abuse in 5, due to pancreas d
ivisum in 1, and of unknown origin in 3. Fifteen patients had severe i
llness and 19 had mild disease. In an patients, total lymphocyte and l
ymphocyte subset counts were carried out on admission, as well as on t
he third and fifth day of hospitalization, using a flow cytometric ana
lysis. Twenty-three patients (13 with severe illness and 10 with mild
disease) also had a repeat count 1 month after recovery. Twenty-five h
ealthy subjects and 27 patients with nonpancreatic acute abdomen compa
rable for sex and age were studied as controls. On the first day of th
e study, the leukocyte number was significantly higher in patients wit
h acute pancreatitis and in those with nonpancreatic acute abdomen wit
h respect to healthy subjects, whereas the number of total and CD4(+)
CD8(+), CD3(+)DR(-), and CD3(-)DR(+) lymphocytes was significantly low
er in acute pancreatitis patients than in healthy subjects or in patie
nts with nonpancreatic acute abdomen. These subset counts persisted on
the third and fifth days of the study. Patients with nonpancreatic ac
ute abdomen and healthy subjects had similar values of total and lymph
ocyte subsets. The patients with acute pancreatitis studied 1 month af
ter complete recovery had numbers of leukocytes, total lymphocytes, an
d CD4(+), CD8(+) CD3(+)DR(-), and CD3(-)DR(+) lymphocytes similar to t
hose in healthy subjects. Regarding CD3(+)DR(+) lymphocytes, the count
in acute pancreatitis patients studied within the first 5 days of hos
pital admission was similar to that in healthy subjects, but 1 month a
fter complete recovery it was significantly higher in the pancreatitis
patients. CD4(+) and CD3(+)DR(-) lymphocyte counts were significantly
lower in patients with severe acute pancreatitis than in patients wit
h mild disease from the third day of illness onward. The CD4(+)-T cell
difference was still present 1 month later. The number of total lymph
ocytes was significantly lower in patients with severe illness relativ
e to those with mild pancreatitis on the fifth day of hospitalization.
Results demonstrate that in early phases of acute pancreatitis there
was a significant decrease in the number of total lymphocytes and lymp
hocyte subset counts relative to controls. These counts returned to no
rmal with resolution of the illness.