Associations of seroreactivity against crystallin proteins with disease activity and cataract in patients with uveitis

Ling Chen, Gary N. Holland, Fei Yu, Ralph D. Levinson, Kirsten Lampi, Joseph Horwitz, Lynn K. Gordon

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

PURPOSE. βB1-crystallin is a putative target of an autoantibody observed in a subset of patients with uveitis. The purpose of this study was to determine whether seroreactivity against βB1 or other specific purified crystallin proteins is observed in patients with uveitis and whether this reactivity is associated with either cataract or active intraocular inflammation. METHODS. Sera from patients with uveitis were tested for IgG antibodies with reactivity against αA-, αB-, βB1-, or βB2-crystallin proteins using a modified slot-blot protocol. Ophthalmic evaluations included analysis of the degree of intraocular inflammation and assessment of lens opacity by the Lens Opacities Classification System (LOCS) III. Positive anti-crystallin reactivity was defined as greater than the mean + 2 SD of the reactivity of a commercially available control serum panel. Statistical analysis was performed with the Fisher exact test, Kruskal-Wallis test, and Student's t-test. RESULTS. IgG antibodies against αA-, αB-, or βB1-crystallin were identified in 70% of 39 subjects; in contrast, only 30% of the control sera exhibited reactivity against one or more of these crystallin proteins (P le; 0.01). Seroreactivity against αA-, αB-, or βB1-, but not βB2-crystallin was related to active anterior segment inflammation. Seroreactivity against αB and βB1 was significantly related to cortical cataract (P ≤ 0.05). CONCLUSIONS. Serum antibodies against specific crystallin proteins are present in most patients with uveitis. The relationship between the presence of specific anti-crystallin antibodies and active inflammation may indicate a role for these autoantibodies in uveitis pathogenesis.

Original languageEnglish (US)
Pages (from-to)4476-4481
Number of pages6
JournalInvestigative Ophthalmology and Visual Science
Volume49
Issue number10
DOIs
StatePublished - Oct 2008

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Crystallins
Uveitis
Cataract
Proteins
Inflammation
Serum
Autoantibodies
Antibodies
Immunoglobulin G
Anti-Idiotypic Antibodies
Students

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems
  • Cellular and Molecular Neuroscience
  • Medicine(all)

Cite this

Associations of seroreactivity against crystallin proteins with disease activity and cataract in patients with uveitis. / Chen, Ling; Holland, Gary N.; Yu, Fei; Levinson, Ralph D.; Lampi, Kirsten; Horwitz, Joseph; Gordon, Lynn K.

In: Investigative Ophthalmology and Visual Science, Vol. 49, No. 10, 10.2008, p. 4476-4481.

Research output: Contribution to journalArticle

Chen, Ling ; Holland, Gary N. ; Yu, Fei ; Levinson, Ralph D. ; Lampi, Kirsten ; Horwitz, Joseph ; Gordon, Lynn K. / Associations of seroreactivity against crystallin proteins with disease activity and cataract in patients with uveitis. In: Investigative Ophthalmology and Visual Science. 2008 ; Vol. 49, No. 10. pp. 4476-4481.
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abstract = "PURPOSE. βB1-crystallin is a putative target of an autoantibody observed in a subset of patients with uveitis. The purpose of this study was to determine whether seroreactivity against βB1 or other specific purified crystallin proteins is observed in patients with uveitis and whether this reactivity is associated with either cataract or active intraocular inflammation. METHODS. Sera from patients with uveitis were tested for IgG antibodies with reactivity against αA-, αB-, βB1-, or βB2-crystallin proteins using a modified slot-blot protocol. Ophthalmic evaluations included analysis of the degree of intraocular inflammation and assessment of lens opacity by the Lens Opacities Classification System (LOCS) III. Positive anti-crystallin reactivity was defined as greater than the mean + 2 SD of the reactivity of a commercially available control serum panel. Statistical analysis was performed with the Fisher exact test, Kruskal-Wallis test, and Student's t-test. RESULTS. IgG antibodies against αA-, αB-, or βB1-crystallin were identified in 70{\%} of 39 subjects; in contrast, only 30{\%} of the control sera exhibited reactivity against one or more of these crystallin proteins (P le; 0.01). Seroreactivity against αA-, αB-, or βB1-, but not βB2-crystallin was related to active anterior segment inflammation. Seroreactivity against αB and βB1 was significantly related to cortical cataract (P ≤ 0.05). CONCLUSIONS. Serum antibodies against specific crystallin proteins are present in most patients with uveitis. The relationship between the presence of specific anti-crystallin antibodies and active inflammation may indicate a role for these autoantibodies in uveitis pathogenesis.",
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AU - Horwitz, Joseph

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N2 - PURPOSE. βB1-crystallin is a putative target of an autoantibody observed in a subset of patients with uveitis. The purpose of this study was to determine whether seroreactivity against βB1 or other specific purified crystallin proteins is observed in patients with uveitis and whether this reactivity is associated with either cataract or active intraocular inflammation. METHODS. Sera from patients with uveitis were tested for IgG antibodies with reactivity against αA-, αB-, βB1-, or βB2-crystallin proteins using a modified slot-blot protocol. Ophthalmic evaluations included analysis of the degree of intraocular inflammation and assessment of lens opacity by the Lens Opacities Classification System (LOCS) III. Positive anti-crystallin reactivity was defined as greater than the mean + 2 SD of the reactivity of a commercially available control serum panel. Statistical analysis was performed with the Fisher exact test, Kruskal-Wallis test, and Student's t-test. RESULTS. IgG antibodies against αA-, αB-, or βB1-crystallin were identified in 70% of 39 subjects; in contrast, only 30% of the control sera exhibited reactivity against one or more of these crystallin proteins (P le; 0.01). Seroreactivity against αA-, αB-, or βB1-, but not βB2-crystallin was related to active anterior segment inflammation. Seroreactivity against αB and βB1 was significantly related to cortical cataract (P ≤ 0.05). CONCLUSIONS. Serum antibodies against specific crystallin proteins are present in most patients with uveitis. The relationship between the presence of specific anti-crystallin antibodies and active inflammation may indicate a role for these autoantibodies in uveitis pathogenesis.

AB - PURPOSE. βB1-crystallin is a putative target of an autoantibody observed in a subset of patients with uveitis. The purpose of this study was to determine whether seroreactivity against βB1 or other specific purified crystallin proteins is observed in patients with uveitis and whether this reactivity is associated with either cataract or active intraocular inflammation. METHODS. Sera from patients with uveitis were tested for IgG antibodies with reactivity against αA-, αB-, βB1-, or βB2-crystallin proteins using a modified slot-blot protocol. Ophthalmic evaluations included analysis of the degree of intraocular inflammation and assessment of lens opacity by the Lens Opacities Classification System (LOCS) III. Positive anti-crystallin reactivity was defined as greater than the mean + 2 SD of the reactivity of a commercially available control serum panel. Statistical analysis was performed with the Fisher exact test, Kruskal-Wallis test, and Student's t-test. RESULTS. IgG antibodies against αA-, αB-, or βB1-crystallin were identified in 70% of 39 subjects; in contrast, only 30% of the control sera exhibited reactivity against one or more of these crystallin proteins (P le; 0.01). Seroreactivity against αA-, αB-, or βB1-, but not βB2-crystallin was related to active anterior segment inflammation. Seroreactivity against αB and βB1 was significantly related to cortical cataract (P ≤ 0.05). CONCLUSIONS. Serum antibodies against specific crystallin proteins are present in most patients with uveitis. The relationship between the presence of specific anti-crystallin antibodies and active inflammation may indicate a role for these autoantibodies in uveitis pathogenesis.

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