Sequential occurrence of thyroid autoantibodies and Graves' disease after immune restoration in severely immunocompromised human immunodeficiency virus-1-infected patients
V. Jubault et al., Sequential occurrence of thyroid autoantibodies and Graves' disease after immune restoration in severely immunocompromised human immunodeficiency virus-1-infected patients, J CLIN END, 85(11), 2000, pp. 4254-4257
We analyzed the kinetics of CD4 cells, human immunodeficiency virus (HIV) v
iral load, and autoantibodies in acquired immune deficiency syndrome patien
ts with Graves' disease (GD) after immune restoration on highly active anti
retroviral therapy (HAART; retrospective study).
Five patients (median age, 41 yr) were diagnosed with GD after 20 (range, 1
4-22) months on HAART on the basis of clinical and biological hyperthyroidi
sm, diffuse hyperfixation of thyroid scan, and the presence of anti-TSH rec
eptor (anti-TSHR) antibodies (Ab). GD was diagnosed several months after th
e plasma HIV ribonucleic acid load became undetectable, when the CD4(+) cel
l count had risen from 14 (range, 0-62) to 340 (range, 163-460) x 10(6) cel
ls/L. Antithyroid peroxidase (anti-TPO) and anti-TSHRAb appeared 14 (range,
9-18) and 14 (range, 11-20) months after starting HAART and 12 (range, 6-1
5) and 11 (range, 9-17) months after the increase in CD4(+) cells. In 3 pat
ients, TPOAb preceded TSHRAb by 3-10 months. No other autoantibodies were d
etected. Thyroid antibodies were absent in a group of 55 HIV-1-positive pat
ients with comparable response to HAART and no symptoms of hyperthyroidism
(cross-sectional study).
Thyroid-specific autoimmunity can occur upon immune restoration with HAART.
Our observations suggest a relationship between thymus-dependent immune re
constitution after immunosuppression and autoimmunity and may provide insig
ht into the pathophysiology of GD.