INT72747
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
The injected IgG was found in the axon terminals of the lumbar ventral horn motor neurons, localizing in the microtubules and rough endoplasmic reticulum. | |||||||||||||||
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If they were pregnant, IgG avidity testing is the preferred method to confirm recent infection,34 because IgM antibodies can persist for months after initial infection in some individuals.35,36 Alternate testing algorithms use higher IgM serologic titers as good indicators of acute infection when economic considerations preempt additional tests.37,38 | |||||||||||||||
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CONCLUSIONS: A radioisotope label on IgG and its visualization in a large series of animal models indicate that a low protein dose of anti-GD2 IgG will not cause neurologic side effects in patients. | |||||||||||||||
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When dimerized with J chain, IgA is actively transported by the polymeric Ig receptor (pIgR) system through the columnar epithelium of conducting airways and is therefore more abundant than IgG in secretions of upper than lower airways [27,28]. | |||||||||||||||
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After its release into airway secretions, secretory M2e(pep-nat)-specific IgA may have lesser protective power than IgG, both in terms of activation of FcR-expressing effector cells and complement. | |||||||||||||||
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Measurement of sera IgG | |||||||||||||||
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For blocking of the cytolytic activity the NK specific antibodies directed against NKp30, NKp44, NKp46 (Immunotech, Marseille, France) and the antibodies directed against Hsp70 (cmHsp70.2, multimmune GmbH) and MICA/B (BAMO1, IgG1; BAMO2, IgG2a, Bamomab, Munich, Germany) on tumor cells were used. | |||||||||||||||
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The FcRn binds pinocytosed IgG only in the acidic environment of the endosome and releases intact IgG when its transport vesicle is redirected to the neutral pH of the cell surface. | |||||||||||||||
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The occurrence of elevated levels of rheumatoid factors (RFs), which are autoantibodies against the Fc portion of IgG molecules, are a diagnostic marker for RA, even though they are not specific for the disease. | |||||||||||||||
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Immunofluorescent antibody staining showed large amounts of both complement protein C3 and IgG in the glomerular mesangium and in the capillary loops (data not shown). | |||||||||||||||
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Using this method, both anti-CCP IgG and anti-tetanus IgG as well as total IgM and IgG were found to be significantly enriched in RA synovia, whereas the value for RF-IgM did not differ significantly from 1. | |||||||||||||||
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Using this method, both anti-CCP IgG and anti-tetanus IgG as well as total IgM and IgG were found to be significantly enriched in RA synovia, whereas the value for RF-IgM did not differ significantly from 1. | |||||||||||||||
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They all had a lower concentration of one or more classes of serum immunoglobulin (IgG, IgM and IgA) than the standard control ranges, and their mean concentration of IgG was significantly lower (P<0.005) than the mean concentration of IgG in 15 clinically normal weimaraners. | |||||||||||||||
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IgM and IgG subclasses were detected using mouse immunoglobulin isotype specific monoclonal antibodies : anti-IgM IgG2a,? | |||||||||||||||
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Representative examples of the data showing IgM responses after primary immunisation, and IgG responses after secondary immunisation, are shown in fig 6 (immunization with 6 ? | |||||||||||||||
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To analyze antibody secretion from sorted YFP+ or plasma cell populations, mouse IgG capture antibodies were coated onto a PVDF-backed microplate. | |||||||||||||||
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We tested the ability of vaults expressing (cp-MVP-z) or lacking (cp-MVP) the Fc binding peptide to adhere to mouse Ig isotypes which are generally found in nasal secretions (IgG and IgA) using an ELISA assay. | |||||||||||||||
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After 4 hours incubation at room temperature, the plates were washed (3 times), and the concentrations of IgG subclass Abs were determined by the addition 100 ? | |||||||||||||||
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In addition, the M2-transduced B cells secreted significantly higher levels of IgG on days 46 post-transduction than the cells transduced with the control retrovirus (Figure 3B). | |||||||||||||||
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EBV encodes a viral IL-10 homolog, BCRF1 (or vIL-10), that has been shown to increase human B cell proliferation following surface immunoglobulin crosslinkinking and induce B cells to secrete increased levels of IgM, IgG, and IgA in a similar manner to cellular IL-10 [17]. | |||||||||||||||
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