Publications by authors named "Jauquline Nordqvist"

Article Synopsis
  • The glycosylation of IgG is important for its interaction with immune cells, and estrogen levels can influence these processes, especially after menopause.
  • Researchers aimed to investigate how estrogen regulates IgG glycosylation in postmenopausal conditions using ovariectomized mice treated with estrogen.
  • The findings indicated that estrogen treatment enhanced certain glycosylation patterns on IgG without affecting overall glycoprotein sialylation, suggesting estrogen plays a role in modulating immune responses through its impact on IgG glycosylation.
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Inflammation has a significant effect on bone remodeling and can result in bone loss via increased stimulation of osteoclasts. Activated immunoglobulins, especially autoantibodies, can increase osteoclastogenesis and are associated with pathological bone loss. Whether immunoglobulins and mature B lymphocytes are important for general bone architecture has not been completely determined.

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Osteoporosis is a common secondary complication in patients with systemic lupus erythematosus (SLE). Current osteoporosis treatment with bisphosphonates has some negative side effects and there is a lack of data regarding newer treatments options for SLE associated osteoporosis. The tissue-selective estrogen complex (TSEC) containing conjugated estrogens and the selective estrogen receptor modulator bazedoxifene (Bza) is approved for treatment of postmenopausal vasomotor symptoms and prevention of osteoporosis.

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Background/objective: 17β-estradiol (E2) has major effects on the immune system. It induces thymic atrophy, inhibits both T and B lymphopoiesis and stimulates antibody production treatment with E2 has protective effects on the skeleton but is associated with negative side effects in reproductive organs. A tissue-selective estrogen complex (TSEC) comprise of estrogens combined with a selective estrogen receptor modulator (SERM).

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