Objective-To report clinical and immunological investigations of contactin-associated proteinlike 2 (Caspr2), an autoantigen of encephalitis and peripheral nerve hyperexcitability (PNH) previously attributed to voltage-gated potassium channels (VGKC).Methods-Clinical analysis of patients with encephalitis, PNH, or both. Immunoprecipitation and mass spectrometry were used to identify the antigen and to develop an assay with Caspr2-expressing cells. Immunoabsorption with Caspr2 and comparative immunostaining of brain and peripheral nerve of wild-type and Caspr2-null mice were used to assess antibody specificity.
An association of TNF with memory, previously reported in patients after exposure to chemotherapy, was found prior to initiation of any treatment, including surgery. This association requires further investigation as sTNF-RII was not higher in cancer patients relative to control participants.
Based on the structural analysis of FIV protease and drug-resistant HIV proteases and molecular
modeling, a new type of inhibitors with a small P3 residue has been developed. These inhibitors are effective
against HIV and its drug-resistant mutants, as well as SIV and FIV. Modification of existing HIV protease
inhibitors by reducing the size of the P3 residue has the same effect. This finding provides a new strategy for
the development of HIV protease inhibitors effective against the wild-type and drug-resistant mutants. It further
supports the use of FIV protease as a useful model for drug-resistant HIV proteases, which often have a more
constricted binding region for the P3 group or the combined P3 and P1 groups.
Results. Mean age was 51 years, 92% were female, 84% were born in Mexico, 55% had sixth grade education or less, and 60% had no medical insurance. Of the 141 participants, 118 completed 6-month followup testing. Repeated-measures analysis of variance showed significant improvement from pretest to 6-month followup in pain (6.0 versus 3.4); self efficacy (5.5 versus 8.4), self-care behavior (1.7 versus 4.9), arthritis knowledge (1.6 versus 4.5), and general health (2.1 versus 2.5), all at P < 0.001. Small improvement was reported in mHAQ (0.56 versus 0.50; P ؍ 0.024). Conclusion. The Spanish Arthritis Empowerment Program was successfully disseminated. Significant improvements in self efficacy and in arthritis symptoms were maintained at the 6-month followup.
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