lymphocyte subpopulations in patients with untreated pernicious anaemia

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CORRESPONDENCE 377 CORRESPONDENCE LYMPHOCYTE SUBPOPULATIONS IN PATIENTS WITH UNTREATED PERNICIOUS ANAEMIA To the Editor: Pernicious anaemia (PA) is generally held to be the result of an autoimmune injury. Alterations in the function and number of immunoregulatory T cells (helper/suppressor) are common in many autoimmune diseases and recently it has been suggested that the imbalance of subsets of lymphocyte may act as a cause of PA by. inducing an autoimmune injury of gastric mucosa (1). Wodzinski et al (2) measured lymphocyte subpopulations and intrinsic factor antibodies in patients with megaloblastic anaemia who were under successful treatment with Vitamine Bt2 injections. The mean T4/T8 ratio vas found to be elevated because of a decrease in the percentage of suppressor cells in 8 of the 10 patients who had intrinsic factor antibodies in their serum. We have investigated blood lymphocytes and the distribution of subsets in 6 patients with untreated PA. All patients had low serum Vitamin B12, mega- loblastic anaemia, atrophic gastritis, achlorhydria and absence of intrinsic factor (IF) secretion before and after pentagastrin. Blocking antibodies against IF were found in the sera of 2 patients, antibodies against parietal-cells in 3, and hypogammaglobulinaemia in 1. All the patients responded to i.m. hydroxycobalamin. The lymphocyte subsets were indentified by the hybridome-produced monoclonal antibodies B1, T4, T8 and T3 (Coulter Immunology, Hialeah, FL), and Leu 7 (Becton-Dickinson, Mountain View, CA). The results are shown in Table 1. We could not demon- strate any alterations in the peripheral blood lympho- cyte subsets, either in percentage or in absolute count. Our patient 3 (with negative intrinsic factor antibodies) TABLE I Lymphocyte subsets (%I in 6 untreated patients with pernicious anaemia T4/T8 T3 T4 T8 Leu 7 B1 ratio PATIENT 1 72 56 20 8 8 2.6 PATIENT 2 80 61 20 ND 6 3.0 PATIENT 3 80 68 16 I1 10 4.2 PATIENT 4 ND 50 16 ND ND 3.1 PATIENT 5 70 60 20 6 6 3.0 PATIENT 6 70 46 18 ND 4 2.4 Normal values in healthyadults(range) 60-75 47-58 17-30 6-15 6-14 1.8-3.1 ND: Not Done had an increased TWT8 ratio and patient 6 had low B-lymphocyte count. Therefore, the T4/T8 imbilance could not be demonstrated. Unlike the patients in other studies (1,2), our patients had not previously been treated when we investigated their lymphocyte sub- populations. Further studies are needed to elucidate exactly the relevance of immunological abnormalities due to cellular-immune mechanisms in patients with PA. References I. Imamura N, Fujimura K, Kurarnoto A. Lymphocyte subpopulations in pernicious anemia. N Engl J Med 1984;311:56. 2. Wodzinski MA, Forrest MJ, Barnett D, Lawrence ACK. Lymphocyte subpopulations in patients with hydroxy- cobalamin responsive megaloblastic anemia. J Clin Pathol 1985;38:582-4. Correspondence to: Jesus Soler, Angel Remacha, Merce Nieto, Enric Gimferrer Department of Haematology Hospital de la Santa Creu i Sant Pau Autonomous University of Barcelona St. Antoni M1 Claret, 167 08025-Barcelona Spain

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Page 1: LYMPHOCYTE SUBPOPULATIONS IN PATIENTS WITH UNTREATED PERNICIOUS ANAEMIA

CORRESPONDENCE 377

CORRESPONDENCE

LYMPHOCYTE SUBPOPULATIONS IN PATIENTS WITH UNTREATED PERNICIOUS ANAEMIA

To the Editor: Pernicious anaemia (PA) is generally held to be the result of an autoimmune injury. Alterations in the function and number of immunoregulatory T cells (helper/suppressor) are common in many autoimmune diseases and recently it has been suggested that the imbalance of subsets of lymphocyte may act as a cause of P A by. inducing an autoimmune injury of gastric mucosa ( 1 ) . Wodzinski et al (2) measured lymphocyte subpopulations and intrinsic factor antibodies in patients with megaloblastic anaemia who were under successful treatment with Vitamine Bt2 injections. The mean T4/T8 ratio vas found to be elevated because of a decrease in the percentage of suppressor cells in 8 of the 10 patients who had intrinsic factor antibodies in their serum. We have investigated blood lymphocytes and the distribution of subsets in 6 patients with untreated PA.

All patients had low serum Vitamin B12, mega- loblastic anaemia, atrophic gastritis, achlorhydria and absence of intrinsic factor (IF) secretion before and after pentagastrin. Blocking antibodies against IF were found in the sera of 2 patients, antibodies against parietal-cells in 3, and hypogammaglobulinaemia in 1. All the patients responded to i.m. hydroxycobalamin.

The lymphocyte subsets were indentified by the hybridome-produced monoclonal antibodies B1, T4, T8 and T3 (Coulter Immunology, Hialeah, FL), and Leu 7 (Becton-Dickinson, Mountain View, CA). The results are shown in Table 1. We could not demon- strate any alterations in the peripheral blood lympho- cyte subsets, either in percentage or in absolute count. Our patient 3 (with negative intrinsic factor antibodies)

TABLE I Lymphocyte subsets (%I in 6 untreated patients with pernicious anaemia

T4/T8 T3 T4 T8 Leu 7 B1 ratio

PATIENT 1 72 56 20 8 8 2.6 PATIENT 2 80 61 20 ND 6 3.0 PATIENT 3 80 68 16 I1 10 4.2 PATIENT 4 ND 50 16 ND ND 3.1 PATIENT 5 70 60 20 6 6 3.0 PATIENT 6 70 46 18 ND 4 2.4

Normal values in healthyadults(range) 60-75 47-58 17-30 6-15 6-14 1.8-3.1

ND: Not Done

had an increased TWT8 ratio and patient 6 had low B-lymphocyte count. Therefore, the T4/T8 imbilance could not be demonstrated. Unlike the patients in other studies (1,2), our patients had not previously been treated when we investigated their lymphocyte sub- populations. Further studies are needed to elucidate exactly the relevance of immunological abnormalities due to cellular-immune mechanisms in patients with PA.

References I . Imamura N, Fujimura K, Kurarnoto A. Lymphocyte

subpopulations in pernicious anemia. N Engl J Med 1984;311:56.

2. Wodzinski MA, Forrest MJ, Barnett D, Lawrence ACK. Lymphocyte subpopulations in patients with hydroxy- cobalamin responsive megaloblastic anemia. J Clin Pathol 1985;38:582-4.

Correspondence to: Jesus Soler, Angel Remacha, Merce Nieto, Enric Gimferrer Department of Haematology Hospital de la Santa Creu i Sant Pau Autonomous University of Barcelona St. Antoni M1 Claret, 167 08025-Barcelona Spain