Autoimmunity and immune system dysregulation in schizophrenia

IgGs from sera of patients hydrolyze myelin basic protein

Daria Parshukova, Liudmila P. Smirnova, Evgeny A. Ermakov, Nikolay A. Bokhan, Arkadiy V. Semke, Svetlana A. Ivanova, Valentina N. Buneva, Georgy A. Nevinsky

Research output: Contribution to journalArticle

Abstract

Several different theories of schizophrenia (SCZ) were discussed; the causes of this disease are not yet clear. Using ELISA, it was shown that titers of autoantibodies against myelin basic protein (MBP) in SCZ patients are ~1.8-fold higher than in healthy individuals but 5.0-fold lower than in patients with multiple sclerosis. Several rigid criteria were checked to show that the MBP-hydrolyzing activity is an intrinsic property of SCZ IgGs. Approximately 82% electrophoretically homogeneous SCZ IgGs purified using several affinity sorbents including Sepharose with immobilized MBP hydrolyze specifically only MBP but not many other tested proteins. The average relative activity of IgGs from patients with negative symptoms was 2.5-fold higher than that of patients with positive symptoms of SCZ, and it increases with the duration of this pathology. It was shown that abzymes are the earliest statistically significant markers of many autoimmune pathologies. Our findings surmise that the immune systems of individual SCZ patients can generate a variety of anti-MBP abzymes with different catalytic properties, which can attack MBP of the myelin-proteolipid shell of axons. Therefore, autoimmune processes together with other mechanisms can play an important role in SCZ pathogenesis. MBP-hydrolyzing antibodies were previously detected in the blood of 80% to 90% of patients with systemic lupus erythematosus (SLE) and multiple sclerosis (MS). In addition, some similar neuropsychiatric indicators of disease common to SLE, MS, and SCZ were described in the literature. Thus, the destruction of the myelin sheath and the production of MBP-hydrolyzing antibodies can be a common phenomenon for some different diseases.

Original languageEnglish
JournalJournal of Molecular Recognition
DOIs
Publication statusAccepted/In press - 1 Jan 2018
Externally publishedYes

Fingerprint

Myelin Basic Protein
Autoimmunity
Immune System
Schizophrenia
Serum
Multiple Sclerosis
Myelin Sheath
Systemic Lupus Erythematosus
Immobilized Proteins
Pathology
Proteolipids
Antibodies
Autoantibodies
Sepharose
Axons
Enzyme-Linked Immunosorbent Assay

Keywords

  • catalytic IgG
  • human blood
  • hydrolysis of myelin basic protein
  • multiple sclerosis
  • schizophrenia
  • systemic lupus erythematosus

ASJC Scopus subject areas

  • Structural Biology
  • Molecular Biology

Cite this

Autoimmunity and immune system dysregulation in schizophrenia : IgGs from sera of patients hydrolyze myelin basic protein. / Parshukova, Daria; Smirnova, Liudmila P.; Ermakov, Evgeny A.; Bokhan, Nikolay A.; Semke, Arkadiy V.; Ivanova, Svetlana A.; Buneva, Valentina N.; Nevinsky, Georgy A.

In: Journal of Molecular Recognition, 01.01.2018.

Research output: Contribution to journalArticle

Parshukova, Daria ; Smirnova, Liudmila P. ; Ermakov, Evgeny A. ; Bokhan, Nikolay A. ; Semke, Arkadiy V. ; Ivanova, Svetlana A. ; Buneva, Valentina N. ; Nevinsky, Georgy A. / Autoimmunity and immune system dysregulation in schizophrenia : IgGs from sera of patients hydrolyze myelin basic protein. In: Journal of Molecular Recognition. 2018.
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abstract = "Several different theories of schizophrenia (SCZ) were discussed; the causes of this disease are not yet clear. Using ELISA, it was shown that titers of autoantibodies against myelin basic protein (MBP) in SCZ patients are ~1.8-fold higher than in healthy individuals but 5.0-fold lower than in patients with multiple sclerosis. Several rigid criteria were checked to show that the MBP-hydrolyzing activity is an intrinsic property of SCZ IgGs. Approximately 82{\%} electrophoretically homogeneous SCZ IgGs purified using several affinity sorbents including Sepharose with immobilized MBP hydrolyze specifically only MBP but not many other tested proteins. The average relative activity of IgGs from patients with negative symptoms was 2.5-fold higher than that of patients with positive symptoms of SCZ, and it increases with the duration of this pathology. It was shown that abzymes are the earliest statistically significant markers of many autoimmune pathologies. Our findings surmise that the immune systems of individual SCZ patients can generate a variety of anti-MBP abzymes with different catalytic properties, which can attack MBP of the myelin-proteolipid shell of axons. Therefore, autoimmune processes together with other mechanisms can play an important role in SCZ pathogenesis. MBP-hydrolyzing antibodies were previously detected in the blood of 80{\%} to 90{\%} of patients with systemic lupus erythematosus (SLE) and multiple sclerosis (MS). In addition, some similar neuropsychiatric indicators of disease common to SLE, MS, and SCZ were described in the literature. Thus, the destruction of the myelin sheath and the production of MBP-hydrolyzing antibodies can be a common phenomenon for some different diseases.",
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AU - Bokhan, Nikolay A.

AU - Semke, Arkadiy V.

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AU - Nevinsky, Georgy A.

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AB - Several different theories of schizophrenia (SCZ) were discussed; the causes of this disease are not yet clear. Using ELISA, it was shown that titers of autoantibodies against myelin basic protein (MBP) in SCZ patients are ~1.8-fold higher than in healthy individuals but 5.0-fold lower than in patients with multiple sclerosis. Several rigid criteria were checked to show that the MBP-hydrolyzing activity is an intrinsic property of SCZ IgGs. Approximately 82% electrophoretically homogeneous SCZ IgGs purified using several affinity sorbents including Sepharose with immobilized MBP hydrolyze specifically only MBP but not many other tested proteins. The average relative activity of IgGs from patients with negative symptoms was 2.5-fold higher than that of patients with positive symptoms of SCZ, and it increases with the duration of this pathology. It was shown that abzymes are the earliest statistically significant markers of many autoimmune pathologies. Our findings surmise that the immune systems of individual SCZ patients can generate a variety of anti-MBP abzymes with different catalytic properties, which can attack MBP of the myelin-proteolipid shell of axons. Therefore, autoimmune processes together with other mechanisms can play an important role in SCZ pathogenesis. MBP-hydrolyzing antibodies were previously detected in the blood of 80% to 90% of patients with systemic lupus erythematosus (SLE) and multiple sclerosis (MS). In addition, some similar neuropsychiatric indicators of disease common to SLE, MS, and SCZ were described in the literature. Thus, the destruction of the myelin sheath and the production of MBP-hydrolyzing antibodies can be a common phenomenon for some different diseases.

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