PubMed Health⌕ Search

PubMed · 14499173

Decrease of B-cells and autoantibodies after low-dose methotrexate.

Abstract

The purpose was to assess the efficacy of low-dose methotrexate (MTX) on immunological parameters in patients with lupus erythematosus (LE) under short- (</=10 weeks) vs. long-term (>10 weeks) conditions. Patients who did not respond to classical LE treatment (antimalarials and/or glucocorticosteroids) were retrospectively analyzed. Twenty-two LE-patients received 10-30 mg MTX per week. Sera and ethylenediaminetetra-acetic blood specimens were analyzed for autoantibodies and lymphocyte subsets (flow cytometry), respectively. Clinical improvement occurred in 21 patients (complete response n = 15, 68.2%). B-cells were the main targets: their absolute number significantly dropped down after long-term treatment (290 +/- 49 vs. 221 +/- 41 microl(-1), P = 0.00254). This was accompanied by down-regulation of autoantibodies. The effect on B-cells was more pronounced in patients with (before vs. long-term 172 +/- 34 vs. 99 +/- 15 microl(-1), P = 0.02853) than without autoantibodies (169 +/- 40 vs. 144 +/- 51 microl(-1), P = 0.55406). MTX did not induce immunosuppression. Low-dose MTX has different short- and long-term effects on immunologic parameters, which could explain the clinical improvement.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Ingrid Böhm. 2003. Decrease of B-cells and autoantibodies after low-dose methotrexate.. https://doi.org/10.1016/s0753-3322(03)00086-6

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Immunostimulatory RNA oligonucleotides trigger an antigen-specific cytotoxic T-cell and IgG2a response.

Single-stranded RNA oligonucleotides containing an immunostimulatory motif (immunostimulatory RNA [isRNA]) are potent inducers of interferon-alpha via the Toll-like receptor 7. We investigated the effect of isRNA on the development of an immune response. We show that isRNA activates dendritic cells and induces production of Th1-type cytokines both in vitro and in vivo. Cytokine production led to bystander activation of T and B cells. We further demonstrate that isRNA triggers the generation of antigen-specific cytotoxic T cells and of an IgG2a-biased antibody response to antigen in a sequence-dependent manner. In summary, we provide evidence for the first time that isRNA oligonucleotides can simultaneously activate the innate and adaptive arms of the immune system.

Adjuvants, Immunologic↗

Mechanism of third signals provided by IL-12 and OX-40R ligation in eliciting therapeutic immunity following dendritic-tumor fusion vaccination.

Dendritic-tumor heterokaryons generated by electrofusion are highly immunogenic. In animal studies, a single vaccination was therapeutic for tumors established in the lung, skin, and brain. However, effective therapy required a third signal which could be provided by exogenous IL-12 or the agonistic anti-OX-40R monoclonal antibody (mAb). In this study, we investigated the mechanism and mode of actions of these two seemingly distinct adjuvants. In immunotherapy of the MCA205 sarcoma, administration of the neutralizing anti-IL-12 mAb nearly completely blocked the adjuvant effect of IL-12, but had minimal inhibitory effects on anti-OX-40R mAb. By contrast, in vivo administration of the antagonistic anti-OX-40L mAb inhibited the adjuvant effects of both IL-12 and anti-OX-40R mAb. Thus, a common pathway of endogenous OX-40 interaction is critical for the development of a therapeutic immune response. Analysis of the third signal mechanism revealed that in the absence of an adjuvant, vaccination with fusion hybrids led to IL-10 production without eliciting IFN-gamma secreting cells. The addition of IL-12 to vaccination suppressed IL-10 production and initiated sensitization of specific IFN-gamma secreting cells, resulting in a type 1-like antitumor immunity. These findings underscore the significance of the third signal in the design of dendritic cell-based cancer vaccines.

Adjuvants, Immunologic↗