Existence of natural mouse IgG mAbs recognising epitopes shared by malondialdehyde acetaldehyde adducts and Porphyromonas gingivalis

Author:

Kyrklund Mikael12,Kaski Heidi1ORCID,Akhi Ramin12,Nissinen Antti E12,Kummu Outi12,Bergmann Ulrich3,Pussinen Pirkko4ORCID,Hörkkö Sohvi12,Wang Chunguang125ORCID

Affiliation:

1. Medical Microbiology and Immunology, Research Unit of Biomedicine, Faculty of Medicine, University of Oulu, Finland

2. Medical Research Centre and Nordlab Oulu, University Hospital and University of Oulu, Finland

3. Protein Analysis Core Facility, Biocentre Oulu and Faculty of Biochemistry and Molecular Medicine, University of Oulu, Finland

4. Oral and Maxillofacial Diseases, University of Helsinki and Helsinki University Hospital, Finland

5. Minerva Foundation Institute for Medical Research, Biomedicum Helsinki 2U, Finland

Abstract

Natural Abs are produced by B lymphocytes in the absence of external Ag stimulation. They recognise self, altered self and foreign Ags, comprising an important first-line defence against invading pathogens and serving as innate recognition receptors for tissue homeostasis. Natural IgG Abs have been found in newborns and uninfected individuals. Yet, their physiological role remains unclear. Previously, no natural IgG Abs to oxidation-specific epitopes have been reported. Here, we show the cloning and characterisation of mouse IgG mAbs against malondialdehyde acetaldehyde (MAA)-modified low-density lipoprotein. Sequence analysis reveals high homology with germline genes, suggesting that they are natural. Further investigation shows that the MAA-specific natural IgG Abs cross-react with the major periodontal pathogen Porphyromonas gingivalis and recognise its principle virulence factors gingipain Kgp and long fimbriae. The study provides evidence that natural IgGs may play an important role in innate immune defence and in regulation of tissue homeostasis by recognising and removing invading pathogens and/or modified self-Ags, thus being involved in the development of periodontitis and atherosclerosis.

Funder

Aarne Koskelon Säätiö

The Finnish Foundation for Cardiovascular Research

Research Fund of Oulu University Hospital/special state support for research

the Research Fund of the Medical Research Center, University of Oulu and Oulu University Hospital

Publisher

SAGE Publications

Subject

Infectious Diseases,Cell Biology,Molecular Biology,Immunology,Microbiology

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