ライフサイエンスコーパス: IgG

1 IgG AHAs cloned from a single human donor exhibited rest

2 IgG antibodies to a novel antigen were elevated in offsp

3 IgG from patients with anti-C3b Abs stabilized C3bBb and

4 IgG MFI was analyzed after elimination of prozone effect

5 IgG titers against glycoprotein (gp) 70V1V2 92TH023 incr

6 IgG transfer in IgG-deficient mice implicated IgG as the

7 ntineuronal nuclear antibody type 1 (ANNA-1) IgG (also known as anti-Hu; 13%).

8 of strikingly different affinities, these 3 IgG subclasses have been shown to enable induction of sy

9 hyl-D-aspartate receptor-IgG and aquaporin-4-IgG coexisted (71%).

10 rare in-frame deletion in FCGR2B abolishing IgG binding to the encoded receptor (p.Asn106del: P = 4.

11 ethod to identify and quantify low-abundance IgG N-glycans and show some of these IgGs can be used as

12 g the impact of the presenting anti-ADAMTS13 IgG antibody and ADAMTS13 antigen on mortality.

13 10-35) of 45 in the placebo group; adjusted IgG seroresponses were seen in 46 (98%, 89-100) of 47 in

14 helper cells and production of high-affinity IgG.

15 on and activation of both CD32 (low affinity IgG receptor) and alphaMss2 integrin.

16 mouse strain in which the human low-affinity IgG receptor locus, comprising both activating (hFcgamma

17 d degranulation of eosinophils on aggregated IgG via increased production and activation of both CD32

18 was true when the autologous and allogeneic IgG concentrations were augmented in allograft recipient

19 nto lamellar nanostructures with alternating IgG and poly(N-isopropylacrylamide) (PNIPAM) nanodomains

20 on in 2015, was 0.024%, equaling amphiphysin IgG (0.026%) and more common than ANNA-2 (also known as

21 agweed-sensitized patients also displayed an IgG response to Amb a 1 isoforms.

22 ally determined the full phase diagram of an IgG antibody.

23 liferation, plasmablast differentiation, and IgG secretion from circulating CD27(+) memory and memory

24 ted to hyposialylation of the Fc glycan, and IgG from T2DM patients was also hyposialylated.

25 ts with delayed meat allergy display IgE and IgG Ab that selectively recognize the alpha-gal epitope

26 We also generated rat IgE and IgG mAbs specific for the folate receptor (FRalpha), whi

27 s were made in parallel to elucidate IgE and IgG reactivity, and putative function analyses were perf

28 IgE and IgG responses to 47 inhalant and food allergen component

29 Binding of IgE and IgG to BGG was confirmed by ELISA and completely abolish

30 HHP treatment decreased the IgE and IgG-binding capacities, indicating a significant decreas

31 Additionally, both HCMV specific IgM and IgG B-cell responses with the ability to neutralize viru

32 provide evidence that although both IgM and IgG BCRs reside in highly heterogeneous protein islands

33 ide association studies for anti-PEG IgM and IgG responses in Han Chinese with 177 and 140 individual

34 Early studies revealed IgM and IgG responses to infection with various filoviruses, but

35 ls, defined as positive for anti-PEG IgM and IgG responses, respectively, and with 492 subjects witho

36 Leptospira-specific IgM and IgG were detected at 15 days postinfection, and isotypin

37 induced by a high fat diet, ex vivo IgM and IgG were elevated with unstimulated B cells.

38 Anti-B19V IgM and IgG, avidity, and ETS assays were used to categorize ind

39 es, reduces total immunoglobulin M (IgM) and IgG levels, and leads to increased proliferation and upr

40 gradual increase of all immunoglobulins and IgG subclasses, but values were always significantly low

41 antigen were specific to ZIKV infection, and IgG avidity revealed recent ZIKV infection and past DENV

42 both IgM (for anti-ATG and anti-Neu5Gc) and IgG (for anti-ATG, -Gal, and -Neu5Gc), peaking at 1 mont

43 ent increased the titers of neutralizing and IgG antibodies against both challenge viruses compared w

44 hey elicited robust GM2-specific overall and IgG antibody responses.

45 developed antibodies and T cells to PAD and IgG antibodies to citrullinated fibrinogen peptides, in

46 , we explored the diversity of protease- and IgG subclass-restricted AHAs and their potential as immu

47 cits significant increases in OPA titers and IgG concentrations that persist 2 years postvaccination

48 nts of IgA-TTG and total IgA, or IgA-TTG and IgG against deamidated gliadin (IgG-DGL) could identify

49 Polyclonal anti-immunoglobulin G (anti-IgG) secondary antibodies are essential tools for many m

50 binding pairs (streptavidin/biotin; IgG/anti-IgG) were quantified.

51 f a coating antibody (Ab), a polyclonal anti-IgG, onto a treated PDMS surface.

52 finity binding between IgG and specific anti-IgG in real-time.

53 or complement activation, reduced antiviral IgG responses to the same extent as observed in mus(-/-)

54 o systemic lupus erythematosus (SLE) non APS IgG.

55 Inclusion criteria were as follows: (1) AQP4-IgG seropositivity, (2) myelitis attack and (3) MRI spin

56 condary antibody labeling of monoclonal AQP4-IgGs with differing epitope specificity bound to isolate

57 nt; 5C8H1 (5/5) more consistently attenuated IgG alloAb production compared to 2C10R4 (4/6) and IDEC-

58 Indeed, balanced IgG signaling through type I and type II Fc receptors is

59 betaPV IgG seroresponses were determined with multiplex serolog

60 ring the kinetic bioaffinity binding between IgG and specific anti-IgG in real-time.

61 a greater than 4-fold increase in HA-binding IgG responses.

62 T cell responses, similar levels of binding IgG antibodies, low levels of IgA antibodies, and high l

63 n-ligand binding pairs (streptavidin/biotin; IgG/anti-IgG) were quantified.

64 technology platform of generating bispecific IgG antibodies, "Bispecific Antibody by Protein Trans-sp

65 series of monovalent and bivalent bispecific IgGs composed of the anti-HER2 trastuzumab moiety paired

66 herapy results in the production of blocking IgG/IgG4 antibodies that can inhibit IgE-dependent activ

67 the induction of allergen-specific blocking IgG in outbred guinea pigs which had been immunized with

68 ning high circulating concentrations of both IgG and albumin.

69 vascular profiles per slice area accessed by IgG by approximately 50%.

70 A mutant strain is predominantly mediated by IgG antibodies binding to antigens expressed exclusively

71 %) LGI1-IgG-positive and 5 of 6 (83%) CASPR2-IgG-positive patients.

72 olvement in patients seropositive for CASPR2-IgG or LGI1-IgG.

73 Cancer was found in 44% of LGI1-IgG/CASPR2-IgG dual seropositive patients (one-third thymoma).

74 on in LGI1-IgG-positive (41%) than in CASPR2-IgG-positive patients (p = 0.033).

75 e in 256 LGI1-IgG-seropositive and/or CASPR2-IgG-seropositive patients.

76 (0.33nmol/l, range = 0.02-5.14) than CASPR2-IgG-positive specimens (0.10nmol/l, range = 0.00-0.45, p

77 on is as follows: CD4(+) T cells/ILC2 cells, IgG, and FcRgamma>mast cells>IgE and FcepsilonRI>basophi

78 d generated from camelid-derived heavy-chain IgGs, are one such example.

79 s had higher voltage-gated potassium channel-IgG immunoprecipitation values (0.33nmol/l, range = 0.02

80 eous binding of IgG, and reduces circulating IgG levels in preclinical animal models.

81 r binding (CMV tet(high) CTLs) in 53/115 CMV IgG(+) patients stem cell transplanted from CMV IgG(+) d

82 Anti-CMV IgG was measured by enzyme-linked immunosorbent assay, a

83 (+) patients stem cell transplanted from CMV IgG(+) donors.

84 Cytomegalovirus (CMV) IgG antibodies have been associated with inflammaging an

85 er of maternal IgG and OVA immune complexes (IgG-IC) via breast milk and induction of allergen-specif

86 d transfer and uptake of allergen-containing IgG immune complexes (Ig-ICs) by gut dendritic cells (DC

87 lin (IVIG) is a FDA-approved drug containing IgG.

88 ollapsin response-mediated protein 5 (CRMP5) IgG (26%) or antineuronal nuclear antibody type 1 (ANNA-

89 e thermodynamic conditions for crystallizing IgG antibodies in the solution environments of interest.

90 had a combination of proximal tubule damage, IgG-positive immune deposits in the tubular basement mem

91 bated with alpha-gal or protein G to deplete IgG Ab. alpha-Gal-specific IgG1-4 Ab in individuals with

92 control of nonspecific human IgG (89)Zr-DFO-IgG in U87MG tumors was 11.5 +/- 3.3 %ID/g, demonstratin

93 The contribution of different IgG isotypes to protection against bacteria such as S.

94 work is needed to define the role different IgG subtypes play in regulating the iatrogenic disease.

95 enopathy, autoantibodies (including anti-DNA IgG), and a type I interferon signature.

96 gM, P < .0001), and anti-double-stranded DNA IgG (P < .05).

97 n a competitive assay or on an indirect EBOV IgG ELISA.

98 Elevated IgG antithyroid AAbs in CSU are linked to the use of glu

99 ntial distribution mechanisms for endogenous IgG, which is one of the most abundant proteins in the C

100 -ICLC increased the low-level serum anti-Env IgG responses elicited by NYVAC-KC priming significantly

101 Patients negative for anti-C3b and anti-FB IgG had much lower rates of infection (17 [25%] patients

102 position 435 (H435) provides for optimal Fc-IgG binding.

103 To monitor IgG Abs, fluoresceinated IgG constant H chain-binding polyclonal F(ab')2 (IgHPoly

104 reflect events documented in vitro following IgG interaction with AQP4: AQP4 internalization, attenua

105 ms (SNPs) for the high affinity receptor for IgG, FcgammaRI.

106 er antigens already validated as targets for IgG suggest a wide potential for development of a novel

107 l clinically defined cohorts were tested for IgG radioimmunoprecipitation of radioiodinated alpha-den

108 Traditional Ab formats (IgG, IgM) are expensive and laborious to produce; howeve

109 We found IgG and anti-CD47 treated tumors resulted in minimal to

110 or both Chlamydia-specific immunoglobulin G (IgG) and polymorphonuclear neutrophils and show the impo

111 Dengue immunoglobulin G (IgG) antibodies were measured at baseline.

112 immunoglobulin M (IgM) and immunoglobulin G (IgG) ELISAs combined can detect ZIKV infection with a se

113 Total immunoglobulin G (IgG) from individuals residing in malaria-endemic region

114 gammaRs), the Fc domain of immunoglobulin G (IgG) mediates a wide spectrum of immunological functions

115 D) ordered arrays of human immunoglobulin G (IgG) were fabricated using well-defined full-length anti

116 d memory B cells and serum immunoglobulin G (IgG).

117 es in the GB1 complex with immunoglobulin G (IgG).

118 nding site and provide new insights into GB1:IgG complex structure that amend and revise the current

119 Rare GFAP-IgG positivity was encountered in serum controls by tiss

120 Here, 102 patients with GFAP-IgG positivity are described.

121 INTERPRETATION: GFAPalpha-IgG, when detected in CSF, is highly specific for an imm

122 IgA-TTG and IgG against deamidated gliadin (IgG-DGL) could identify patients with and without celiac

123 rotocol, native heterogeneously glycosylated IgG N-glycans are first deglycosylated with a wild-type

124 the cross-linked Env group developed higher IgG responses against a linear epitope in the gp120 C1 r

125 ge by converting a promiscuous natural human IgG-binding domain, the hyperthermophilic variant of pro

126 1.3 %ID/g and a control of nonspecific human IgG (89)Zr-DFO-IgG in U87MG tumors was 11.5 +/- 3.3 %ID/

127 ysins can be fused to the Fc region of human IgG, creating a fully functional homodimer (or "lysibody

128 ived only vaginal vaccinations had identical IgG but superior IgA responses.

129 so tested 6 to 12 months before the event if IgG dnDSA was present.

130 cated 5 known variants associating with IgA, IgG or IgM levels or with composite immunoglobulin trait

131 xpression and surface bound antibodies (IgE, IgG) were quantified on basophils.

132 Total and allergen-specific IgE, IgG and basophil sensitivity were measured before and 8

133 rgens, hydrolase activity and detectable IgE/IgG reactivity are strongly correlated, while no protein

134 , and investigate their correlation with IgE/IgG responses and protein function.

135 EIAs in the United States, the combined IgM/IgG Vidas test (LYT).

136 significant decrease of all immunoglobulins, IgG subclasses and pneumococcal polysaccharide antibodie

137 gG transfer in IgG-deficient mice implicated IgG as the pathogenetic ligand for endothelial FcgammaRI

138 ve B cell repertoire but are rarely found in IgG memory B cells from healthy individuals.

139 dy observed sparse lymphocytic infiltrate in IgG-treated tumors and increased inflammatory cell infil

140 ealthy subjects caused insulin resistance in IgG-deficient mice via FcgammaRIIB, indicating that simi

141 n WT amniotic fluid (AF) were higher than in IgG-free AF of B cell-deficient dams.

142 IgG transfer in IgG-deficient mice implicated IgG as the pathogenetic li

143 py-induced antibodies, sensitization-induced IgG did not show IgE-blocking activity.

144 ion is negatively regulated by an inhibitory IgG-receptor.

145 (ab')2 fragments and did not bind the intact IgG counterpart.

146 re important for B cell differentiation into IgG-producing PC.

147 anti-insulin antibody in the presence of its IgG isotype.Efficient detection of single molecules is v

148 cular access and distribution of full-length IgG could be enhanced by intrathecal co-infusion of hype

149 resulted in 30% of human samples having less IgG and IgM RBC xenoreactivity than alloreactivity.

150 LGI1-IgG-positive specimens had higher voltage-gated potassiu

151 pectrum and longitudinal outcome in 256 LGI1-IgG-seropositive and/or CASPR2-IgG-seropositive patients

152 testing, detecting only 24 of 38 (63%) LGI1-IgG-positive and 5 of 6 (83%) CASPR2-IgG-positive patien

153 poral hyperintensity was more common in LGI1-IgG-positive (41%) than in CASPR2-IgG-positive patients

154 Cancer was found in 44% of LGI1-IgG/CASPR2-IgG dual seropositive patients (one-third thy

155 patients seropositive for CASPR2-IgG or LGI1-IgG.

156 s system (PNS) manifestations, 39% were LGI1-IgG seropositive (7% had solely neuropathy or pain).

157 Initial viral load, IgG, and initial neutralization response were assayed an

158 ensitized patients were tested using Luminex IgG-SAB and C1q-SAB assays.

159 an immunological perspective in maintaining IgG populations, FcRn can contribute to the pathogenesis

160 n and developed fewer spleen and bone marrow IgG plasma cells and memory B cells, compared with contr

161 pecimens from contact bats, followed by MARV IgG antibodies in these same bats.

162 ceptor (FcRn)-dependent transfer of maternal IgG and OVA immune complexes (IgG-IC) via breast milk an

163 The presence of maternal IgG antibody specific to respiratory syncytial virus is

164 t the 2 x 10(7) PFU dose, the geometric mean IgG ELISA endpoint titre was 1624 (95% CI 1146-2302) and

165 resumptive pulmonary tuberculosis to measure IgG antibody responses to 57 M. tuberculosis antigens us

166 o or more sites and linear basement membrane IgG or C3).

167 MOG-IgG serostatus was longitudinally assessed in seropositi

168 ndrocyte glycoprotein immunoglobulin G1 (MOG-IgG) and associated clinical features of patients from a

169 follow-up suggested that persistence of MOG-IgG is associated with relapses.

170 so investigate the clinical relevance of MOG-IgG through a longitudinal analysis of serological statu

171 most commonly observed in patients with MOG-IgG.

172 To monitor IgG Abs, fluoresceinated IgG constant H chain-binding po

173 Moreover, IgG transferred from patients with T2DM but not from met

174 36 patients with BP without anti-BP180 NC16A IgG reactivity underwent evaluation of the diagnostic im

175 In children anti-Neu5Gc IgG levels correlated positively with living on a farm a

176 hat initial high viral load and neutralizing IgG response may function in a seemingly contrasting man

177 T by helping B cells to produce neutralizing IgG antibodies.

178 enous immunoglobulin (IVIG), a pooled normal IgG formulation prepared from thousands of healthy donor

179 Monocytes responded to IgE but not IgG exposure by upregulating TNFalpha, which in turn ind

180 Addition of DENV1-NS1 IgG ELISA can distinguish primary ZIKV infection; the ra

181 ratio of absorbance of ZIKV-NS1 to DENV1-NS1 IgG ELISA can distinguish ZIKV with previous DENV and se

182 The ZIKV-NS1 IgG cross-reactivity by samples from secondary DENV infe

183 The magnitude, longevity and avidity of IgG differed significantly among mouse strains.

184 yeloid cells and its differential binding of IgG subclasses controls the contributions of mast cells,

185 dic pH, prevents the simultaneous binding of IgG, and reduces circulating IgG levels in preclinical a

186 Crystallization of IgG antibodies has important applications in the fields

187 and the liquid-liquid coexistence curve, of IgG antibodies.

188 Serum DSA levels and the deposition of IgG and C4d in the allograft were equivalent in the 2 gr

189 immune cell infiltrates, or the deposits of IgG and complement in the kidney.

190 In systemic lupus erythematosus, deposits of IgG-immune complexes and the activation of complement in

191 eutic approaches for limiting the effects of IgG-mediated autoimmune disease.

192 h CSU exhibit significantly higher levels of IgG antithyroid AAbs (strong evidence) and IgE-anti-TPO

193 Levels of IgG antithyroid AAbs are more often elevated in adult pa

194 rong link between CSU and elevated levels of IgG antithyroid autoantibodies (AAbs), with most of a la

195 The levels of IgG response among participants varied significantly acc

196 nitiating the pathophysiological outcomes of IgG binding to astrocytic AQP4 are poorly understood.

197 served (r = 0.481; P = .31), the presence of IgG anti-BP180 NC16A antibodies was associated with the

198 lymphocytes in SLE beyond the production of IgG autoantibodies.

199 o resulted in HLA-DR-dependent production of IgG with anti-vimentin specificities.

200 IgG subtypes and (iii) assess reactivity of IgG antibodies against proteins modified to different le

201 ating prolonged trans-intestinal transfer of IgG.

202 efeldin A treatment did not affect uptake of IgG-coated latex beads.

203 is required to explore the potential use of IgG FXa reactivity as a novel biomarker to stratify trea

204 Monoclonal gammopathy was of IgG type in 47 (94%) patients.

205 plays a critical role in the trafficking of IgGs across tissue barriers and in retaining high circul

206 e the authors conduct a multivariate GWAS on IgG N-glycosylation phenotypes and identify 5 novel loci

207 ivity to systemic anaphylaxis that relies on IgG Fc receptors (FcgammaRs).

208 o His6-OPH in vivo as determined by anti-OPH IgG and cytokines formation in Sprague Dawley rats and B

209 492 subjects without either anti-PEG IgM or IgG as controls.

210 cted in 86%; the remainder had IgM lambda or IgG kappa.

211 s already been successfully applied to other IgG-based therapeutics, substantially improving their cl

212 Application of OVA/IgG immune complexes during pregnancy boosted OVA uptake

213 ison of experimentally mapped Der f 1/Der p1 IgG epitopes to the same surface patch on Blo t 1, as we

214 ialylation was highly specific to pathogenic IgG at the site of inflammation, driven by local platele

215 A minority (17.5%) of patients' IgG also bound to MAP1A.

216 Normal plasma IgG contains approximately 94% fucosylated Abs, but allo

217 the dual combination promoted Th1-polarized IgG responses.

218 Neither in vivo anti- Pp IgG antibody nor in vitro anti- Pp T-cell response and r

219 f autoantibodies in five patients presenting IgG reactivity against the nodes of Ranvier.

220 sharp pH changes in order to mimic properly IgGs Fc domain/FcRn receptor interaction.

221 to increase the average mass of proteolytic IgG peptides (>/=4.5 kDa) and produce peptides which uni

222 (64)Cu-NODAGA-PSMA-IgG and (64)Cu-NODAGA-PSMA-Mb retained the ability to bi

223 travenous immunoglobulin (IVIG) are purified IgG preparations made from the pooled plasma from thousa

224 Mice injected with purified IgG from rabbit serum that was taken before immunization

225 Purified IgGs from residents in malaria endemic areas have shown

226 jection, and immunohistochemistry for rabbit IgG and THSD7A as well as ultrastructural analyses showe

227 Analysis of EHV-1-reactive IgG subtypes demonstrated that vaccination with the VC2-

228 ice and rabbits, MBC4 induced cross-reactive IgG antibodies, which were able to block the binding of

229 lar Ca(2+) release in HUVEC and FXa reactive IgG from patients with APS and/or SLE potentiate this ef

230 vation and investigated whether FXa reactive IgG from patients with APS or SLE/APS- alter these respo

231 Factor (F) Xa reactive IgG isolated from patients with antiphospholipid syndrom

232 In contrast to IgM cross-reactivity, IgG and IgA antibodies against ZIKV nonstructural protei

233 best when both N-methyl-D-aspartate receptor-IgG and aquaporin-4-IgG coexisted (71%).

234 In conclusion, AHAs specifically recognize IgG subclass- and protease-restricted hinge neoepitopes.

235 id precursor N-acetyl-D-mannosamine restored IgG sialylation and preserved insulin sensitivity withou

236 produced V-gene-matched recombinant anti-RhD IgG Abs of the four different subclasses (IgG1-4) with a

237 o developed CL presented higher anti-rLinB13 IgG responses, before the appearance of clinical symptom

238 but not controls, were stimulated to secrete IgG and increase CD27 expression when cultured with solu

239 r1g in non-B cells, we transferred anti-self-IgG (rheumatoid factor) B cells and their physiologic ta

240 e brain and globally despite decreased serum IgG levels.

241 duced detectable Dengue cross-reactive serum IgG responses that significantly amplified after Dengue-

242 y 10-fold higher CT B subunit-specific serum IgG response in IgA(-/-) mice after CT immunization was

243 Vaccination induced significant IgG responses for all serotypes: at day 30 compared with

244 inst HSV-1 is deemed limited due to the slow IgG diffusion rate in the healthy cornea.

245 hese findings suggest that allergen-specific IgG antibodies can act to induce and sustain immunologic

246 els have demonstrated that allergen-specific IgG confers sensitivity to systemic anaphylaxis that rel

247 Allergen-specific IgG was administered to mice undergoing sensitization an

248 ked differences between regions and specific IgG (>/=0.5 ISU) was present in most subjects everywhere

249 l animals exhibited mucosal antigen-specific IgG and IgA with the IgA responses 30-fold greater than

250 l responses, (ii) characterize drug-specific IgG subtypes and (iii) assess reactivity of IgG antibodi

251 ectable HAI-antibodies but high flu-specific IgG-antibody titers mounted rapid functional antibodies

252 Food-specific IgG antibodies arise in the setting of naturally resolvi

253 gG Ab nor the addition of alpha-gal-specific IgG Ab from nonallergic individuals changed the IgE reco

254 e depletion of autologous alpha-gal-specific IgG Ab nor the addition of alpha-gal-specific IgG Ab fro

255 nogenic in humans and causes glycan-specific IgG and also IgE responses with clinical relevance.

256 residues was used to detect hapten-specific IgG 1-4 subclasses in patient plasma.

257 lf-reactive antibodies and parasite-specific IgG in female Soay sheep.

258 munization schemes that induce Pn3P-specific IgG responses in a carbohydrate-specific T cell-dependen

259 e magnitudes of the gp120- and V1V2-specific IgG responses were comparable between adults and infants

260 potentially protective maternal V3-specific IgG antibodies associated with reduced peripartum HIV tr

261 For other antigens, variant-specific IgG titers do not predict colonization.

262 ificant correlation between antigen-specific IgGs for longevity but not for magnitude and avidity.

263 th 10-fold lower titers and antigen-specific IgGs, (anti-HBs, anti-HBc), consistent with partial immu

264 ry despite marked activation and spontaneous IgG production by intrahepatic B cells.

265 The Bioplex 2200 Syphilis IgG immunoassay displayed a similar PPA (100%) but a sub

266 ay was compared to the Bioplex 2200 Syphilis IgG multiplex flow immunoassay.

267 We show that IgG N-glycosylation loci are strongly enriched for genes

268 d N-glycan substrates, 3-4 d to engineer the IgG N-glycosylation, and 2-5 d to synthesize the small-m

269 ortant for uptake of most cargos, except the IgG-coated ones.

270 In mice, the IgG subclass induced after Ag encounter can reflect the

271 ses of both the magnitude and avidity of the IgG binding response than those with Env protein alone.

272 ed to assess the biological relevance of the IgG microheterogeneities thus providing valuable informa

273 anti-EPX and anti-nuclear antibodies of the IgG subtype.

274 Interaction of the IgG-AQP4 complex with FcgammaRs triggers coendocytosis o

275 Distinct glycoforms on the IgG crystallizable fragment (Fc) dictate these divergent

276 of 46 serum samples) when combined with the IgG anti-BP180 enzyme-linked immunosorbent assay.

277 for the generation of bispecific therapeutic IgGs of which several have progressed into the clinic.

278 undance IgG N-glycans and show some of these IgGs can be used as biomarkers for rheumatoid arthritis.

279 L/6 mice with CPS-CRM197 produced high-titer IgG and opsonizing antibody responses against the CPS co

280 ation with Hcp1 and TssM produced high-titer IgG and robust gamma interferon-secreting T cell respons

281 ctive mechanism derives from FcRn binding to IgG in the weakly acidic environment contained within en

282 ased in anti-CD47 treated tumors compared to IgG control.

283 gh it is known that CH1 folding is linked to IgG assembly and secretion.

284 , basophils, neutrophils, and macrophages to IgG subclass-dependent anaphylaxis.

285 ctors underlying differential sensitivity to IgG-mediated arthritis in 2 mast cell-deficient murine l

286 ization resulted in higher serological total IgG, IgG1, and IgG2a anti-alpha-syn levels.

287 esults revealed that the titers of the total IgG and subtype IgG1 anti-SjHSP60 antibodies were positi

288 ing of the Ig subclass showed that the total IgG response switched from an IgG1 response to an IgG3 r

289 At transplantation, total IgG and HLA antibodies were eliminated.

290 -magnitude, potentially protective anti-V1V2 IgG responses than in adult vaccinees receiving the mode

291 Circulating anti-vimentin IgG autoantibody levels were much greater in IPF subject

292 mmaRIIIA binding, in vitro ADCC, and in vivo IgG-mediated cellular depletion, regardless of sialylati

293 uoresceinated secondary Ab (2nd-Ab), whereas IgG subclasses are monitored with Fc-specific monoclonal

294 matopoietic and parenchymal cells, whereupon IgG is diverted from degradation in lysosomes and is rec

295 monitored with Fc-specific monoclonal whole IgG (FcMonoIgG).

296 aled that LRP2 specifically colocalized with IgG in the tubular immune deposits on the ABBA biopsy sp

297 th biclonal gammopathy multiple myeloma with IgG or IgA MGUS clones were subsequently identified from

298 Nanoparticles comparable in size with IgG dimers do not permeate into it.

299 he current model available from studies with IgG fragments.

300 zed mothers or maternal supplementation with IgG-IC was sufficient to induce neonatal tolerance.