Different systemic and local responses to mycobacterial antigens suggest an
active compartmentalization of responsive lymphocytes to tubercular antige
ns. This fact, observed in pleuritic processes, raises doubts about the acc
uracy of information obtained in the study of cells taken solely from perip
heral blood. For this reason we decided to study the concept of compartment
alization in 140 patients suffering from pleural effusions. Patients were c
lassified into six groups according to the aetiology of the effusion: group
I, tuberculous, n = 23; group II, paraneoplastic, n = 41; group III, metap
neumonic empyematous, n = 5; group IV, transudate, n = 38; group V, miscell
aneous exudate, n = 19; group VI, unknown aetiology, n = 14. In each group
we studied the lymphocyte population by using flow cytometry with doubly fl
uorescent monoclonal antibodies: B [expressing human lymphocyte antigen (HL
A)-DR on the surface], T (CD3 +), CD4 + and CD8 +, and the subpopulation of
activated T lymphocytes (together expressing CD3 and HLA-DR on the surface
) (CD3 + DR +). The study of these subpopulations in peripheral blood did n
ot yield valuable results, but the CD3 + DR + population in pleural fluid d
emonstrated a diagnostic efficiency of 84% [positive predictive value (PPV)
51%, negative predictive value (NPV) 96%] at a cut-off value of 80.4 cells
/mm(3). The CD3 + DR + pleural fluid/peripheral blood ratio demonstrated an
efficiency of 83% (PPV 50%, NPV 96%), and showed a statistically significa
nt difference (P < 0.02) with regard to all the diagnostic groups, with the
exception of the paraneoplastic effusions. The lymphocytic subpopulations
study confirms the concept of compartmentalization in tuberculous pleuritis
, as shown by the greater number of activated T lymphocytes present in pleu
ral fluid in comparison with peripheral blood in tuberculous pleuritis, a 9
8% efficiency of adenosine deaminase (ADA) determination in pleural fluid v
ersus a 50% value in peripheral blood, predominance of helper cells (CD4 +)
in pleural fluid and suppressor cells (CD8 +) in peripheral blood, a great
er CD4 +/CD8 + ratio in pleural fluid than in peripheral blood, and a signi
ficant correlation of ADA-CD3 + DR + in pleural fluid, which does not occur
in peripheral blood.