<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Infection and Immunity</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Infection and Immunity</journal-title><trans-title-group xml:lang="ru"><trans-title>Инфекция и иммунитет</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2220-7619</issn><issn publication-format="electronic">2313-7398</issn><publisher><publisher-name xml:lang="en">SPb RAACI</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">138</article-id><article-id pub-id-type="doi">10.15789/2220-7619-2013-4-301-310</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">AUTOREACTIVE ANTIBODIES IN A HEALTHY HUMAN AND IN PATIENTS WITH VIRAL INFECTIONS</article-title><trans-title-group xml:lang="ru"><trans-title>АУТОРЕАКТИВНЫЕ АНТИТЕЛА В НОРМЕ И ПРИ ВИРУСНЫХ ИНФЕКЦИЯХ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Krivitskaya</surname><given-names>V. Z.</given-names></name><name xml:lang="ru"><surname>Кривицкая</surname><given-names>В. З.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>PhD, MD (Biology), Leading Researcher, Laboratory of Biotechnology</p><p>197376, Russian Federation, St. Petersburg, Professor Popov str., 15/17</p></bio><bio xml:lang="ru"><p>д.б.н., ведущий научный сотрудник лаборатории биотехнологии</p><p>197376, Россия, Санкт-Петербург, ул. Профессора Попова, 15/17</p></bio><email>vera.kriv@influenza.spb.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Research Institute of Influenza, Ministry of Health of the Russian Federation, St. Petersburg</institution></aff><aff><institution xml:lang="ru">ФГБУ НИИ гриппа МЗ РФ, Санкт-Петербург</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2013-07-08" publication-format="electronic"><day>08</day><month>07</month><year>2013</year></pub-date><volume>3</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>301</fpage><lpage>310</lpage><history><date date-type="received" iso-8601-date="2014-07-08"><day>08</day><month>07</month><year>2014</year></date><date date-type="accepted" iso-8601-date="2014-07-08"><day>08</day><month>07</month><year>2014</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2014, Krivitskaya V.Z.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2014, Кривицкая В.З.</copyright-statement><copyright-year>2014</copyright-year><copyright-holder xml:lang="en">Krivitskaya V.Z.</copyright-holder><copyright-holder xml:lang="ru">Кривицкая В.З.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://iimmun.ru/iimm/article/view/138">https://iimmun.ru/iimm/article/view/138</self-uri><abstract xml:lang="en"><p><bold>Abstract.</bold> This brief review presents the data obtained during the last two decades which allow to create a new view on autoimmunity. Regulatory and protective characteristics of autoreactive natural antibodies and their role in development of effective adaptive antiviral immune response are discussed. The article considers the problem of possible autoimmune complications due to some viral infections and antiviral vaccination.</p></abstract><trans-abstract xml:lang="ru"><p><bold>Резюме.</bold> В кратком обзоре литературы представлены данные последних двух десятилетий, позволившие сформировать новый взгляд на роль аутоиммунных процессов в жизнедеятельности организма человека. Рассмотрен вопрос о регуляторных и протективных свойствах аутореактивных нормальных антител, а также их роли в формировании эффективного адаптивного противовирусного иммунного ответа. Обсуждается проблема возможных аутоиммунных осложнений некоторых вирусных заболеваний и противовирусной вакцинации.</p></trans-abstract><kwd-group xml:lang="en"><kwd>autoreactive antibodies</kwd><kwd>natural antibodies</kwd><kwd>polyspecificity</kwd><kwd>innate immunity</kwd><kwd>adaptive immune response</kwd><kwd>viral infections</kwd><kwd>antiviral vaccination</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>аутореактивные антитела</kwd><kwd>нормальные антитела</kwd><kwd>полиспецифичность, врожденный иммунитет</kwd><kwd>адаптивный иммунный ответ</kwd><kwd>вирусные инфекции</kwd><kwd>противовирусная вакцинация</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>1.	Кривицкая В.З., Сверлова М.В., Суховецкая В.Ф., Львов Н.И., Васильева И.A., Соминина А.А. Выявление аутореактивных антител класса М у пациентов с респираторными вирусными инфекциями // Медицинская иммунология. — 2008. — Т. 10, № 2–3. — С. 229–238. Krivitskaya V.Z., Sverlova M.V., Sukhovetskaya V.F., L`vov N.I., Vasil`eva I.A., Sominina A.A. Vyyavlenie autoreaktivnykh antitel klassa M u patsientov s respiratornymi virusnymi infektsiyami [Detection of autoreactive immunoglobulin M in patients affected by respiratory viral infections]. Meditsinskaya immunologiya — Medical Immunology, 2008, vol. 10, no. 2–3, pp. 229–238.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>2.	Кривицкая В.З. Характеристика аутореактивных антител класса IgG у пациентов с острыми респираторными вирусными инфекциями // Цитокины и воспаление. — 2011. — Т. 10, № 2. — С. 21–27. Krivitskaya V.Z. Harakteristika autoreaktivnykh antitel klassa IgG u patsientov s ostrymi respiratornymi virusnymi infektsiyami [Autoreactive immunoglobulin G antibody response in patients with acute respiratory viral infections]. Tsitokiny i vospalenie — Citokines and Inflammation, 2011, vol. 10, no. 2, pp. 21–27.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>3.	Adeyi O.A. Vascular and glomerular manifestations of viral hepatitis B and C: a review. Semin. Diagn. Pathol., 2009, vol. 26, no. 2, pp. 116–121.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>4.	Baker N., Ehrenstein M. Cutting edge: selection of B lymphocyte subsets is regulated by natural IgM. J. Immunol., 2002, vol. 169, no. 12, pp. 6686–6690.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>5.	Baumgarth N., Herman O., Jager G., Brown L., Herzenberg L., Chen J. B-1 and B-2 cell-derived immunoglobulin M antibodies are nonredundant components of the protective response to influenza virus infection. J. Exp. Med., 2000, vol. 192, no. 2, pp. 271–280.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>6.	Baumgarth N., Tung J., Herzenberg L. Inherent specificities in natural antibodies: a key to immune defense against pathogen invasion. Springer Semin. Immunopathol., 2005, vol. 26, no. 4, pp. 347–362.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>7.	Bhol K., Natarajan K., Nagarwalla N., Mohimen A., Aoki V., Ahmed A.R. Correlation of peptide specificity and IgG subclass with pathogenic and nonpathogenic autoantibodies in pemphigus vulgaris: a model for autoimmunity. Proc. Natl. Acad. Sci. USA, 1995, vol. 92, no. 11, pp. 5239–5243.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>8.	Boes M., Esau C., Fischer M., Schmidt T., Carroll M., Chen J. Enhanced B-1 cell development, but impaired IgG antibody responses in mice deficient in secreted IgM. J. Immunol., 1998, vol. 160, pp. 4776–4787.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>9.	Boes M., Schmidt T., Linkemann K., Beaudette B., Marshak-Rothstein A., Chen J. Accelerated development of IgG autoantibodies and autoimmune disease in the absence of secreted IgM. Proc. Natl. Acad. Sci. USA, 2000, vol. 97, no. 3, pp. 1184–1189.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>10.	Bonagura V., Agostino N., Borretzen M., Thompson K., Natvig J., Morrison S. Mapping IgG epitopes bound by rheumatoid factors from immunized controls identifies disease-specific rheumatoid factors produced by patients with rheumatoid arthritis. J. Immunol., 1998, vol. 160, no. 5, pp. 2496–2505.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>11.	Brändlein S., Pohle T., Ruoff N., Wozniak E., Müller-Hermelink H.-K., Vollmers H. Natural IgM antibodies and immunosurveillance mechanisms epithelial cancer cells in humans. Cancer Res., 2003, vol. 63, pp. 7995–8005.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>12.	Cabiedes J., Cabral A., Lopez-Mendoza A., Cordero-Esperon A., Huerta M., Alarcon-Segovia D. Characterization of anti-phosphatidylcholine polyreactive natural utoantibodies from normal human subjects. J. Autoimmun., 2002, vol. 18, no. 2, pp. 181–190.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>13.	Craig M.E., Nair S., Stein H., Rawlinson W.D. Viruses and type 1 diabetes: a new look at an old story. Pediatr. Diabetes., 2013, vol. 14, no. 3, pp. 149–158.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>14.	Drexler S.K., Foxwell B.M. The role of Toll-like receptors in chronic inflammation. Int. J. Biochem. Cell Biol., 2010, vol. 42, no. 4, pp. 506–518.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>15.	Dumoulin F., Leifeld L., Sauerbruch T., Spengler U. Autoimmunity induced by interferon-alpha therapy for chronic viral hepatitis. Biomed. Pharmacother., 1999, vol. 53, no. 5–6, pp. 242–254.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>16.	Ehrenstein M., Katz D., Griffiths M., Papadaki L., Winkler T., Kalden J.,Isenberg D. Human IgG anti-DNA antibodies deposit in kidneys and induce proteinuria in SCID mice. Kidney Int., 1995, vol. 48, no. 3, pp. 705–711.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>17.	Ercolini A.M., Miller S.D. The role of infections in autoimmune disease. Clin. Exp. Immunol., 2009, vol. 155, no. 1, pp. 1–15.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>18.	Evans D., Cauchemez S., Hayden F.G. «Prepandemic» immunization for novel influenza viruses, «swine flu» vaccine, Guillain–Barré syndrome, and the detection of rare severe adverse events. J. Infect. Dis., 2009, vol. 200, no. 3, pp. 321–328.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>19.	Fehr T., Bachmann M.F., Bucher E., Kalinke U., Di Padova F.E., Lang A.B., Hengartner H., Zinkernagel R.M. Role of repetitive antigen patterns for induction of antibodies against antibodies. J. Exp. Med., 1997, vol. 185, no. 10, pp. 1785–1792.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>20.	Forster J., Maier O., Löbbert J., Kaufmehl K., Streckert H.J., Werchau H. Prevalence of antibodies against HEp-2 cell antigen in infants and children hospitalized with respiratory syncytial virus infection. Infection, 1996, vol. 24, no. 6, pp. 407–411.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>21.	Fujinami R.S., von Herrath M.G., Christen U., Whitton J.L. Molecular mimicry,bystander activation, or viral persistence: infections and autoimmune disease. Clin. Microbiol. Rev., 2006, vol. 19, no. 1, pp. 80–94.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>22.	Grönwall C., Vas J., Silverman G.J. Protective Roles of Natural IgM Antibodies. Front. Immunol., 2012, vol. 3, article 66.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>23.	Guglielmone H., Vitozzi S., Elbarcha O., Fernandez E. Cofactor dependence and isotype distribution of anticardiolipin antibodies in viral infections. Ann. Rheum. Dis., 2001, vol. 60, no. 5, pp. 500–504.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>24.	Hahm K., Im Y., Lee C., Parks W., Bang Y., Green J., Kim S. Loss of TGF-beta signaling contributes to autoimmune pancreatitis. J. Clin. Invest., 2000, vol. 105, no. 8, pp. 1057–1065.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>25.	Hasegawa M., Fujimoto M., Takehara K., Sato S. Pathogenesis of systemic sclerosis: altered B cell function is the key linking systemic autoimmunity and tissue fibrosis. J. Dermatol. Sci., 2005, vol. 39, no. 1, pp. 1–7.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>26.	Kaiser L., Fritz R., Straus S., Gubareva L., Hayden F. Symptom pathogenesis during acute influenza: interleukin-6 and other cytokine responses. J. Med. Virol., 2001, vol. 64, no. 3, pp. 262–268.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>27.	Kajon A., Gigliotti A., Harrod K. Acute inflammatory response and remodeling of airway epithelium after subspecies B1 human adenovirus infection of the mouse lower respiratory tract. J. Med. Virol., 2003, vol. 71, no. 2, pp. 233–244.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>28.	Kaveri S.V. Intravenous immunoglobulin: exploiting the potential of natural аntibodies. Autoimmun Rev., 2012, vol. 11, no. 11, pp. 792–794.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>29.	Kerr J., Barah F., Mattey D., Laing I., Hopkins S., Hutchinson I., Tyrrell D. Circulating tumour necrosis factor-alpha and interferon-gamma are detectable during acute and convalescent parvovirus B19 infection and are associated with prolonged and chronic fatigue. J. Gen. Virol., 2001, vol. 82, pt. 12, pp. 3011–3019.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>30.	Kim J. Identification of a human monoclonal natural IgM antibody that recognizes early poptotic cells and promotes phagocytosis. Hybridoma (Larchmt), 2010, vol. 29, no. 4, pp. 275–281.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>31.	Kobayashi N., Bagheri N., Nedrud J., Strieter R., Tomino Y., Lamm M., Emancipator S. Differential effects of Sendai virus infection on mediator synthesis by mesangial cells from two mouse strains. Kidney Int., 2003, vol. 64, no. 5, pp. 1675–1684.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>32.	Korganow A.S, Ji H., Mangialaio S., Duchatelle V., Pelanda R., Martin T., Degott C., Kikutani H., Rajewsky K., Pasquali J.L., Benoist C., Mathis D. From systemic T cell self-reactivity to organ-specific autoimmune disease via immunoglobulins. Immunity, 1999, vol. 10, no. 4, pp. 451–461.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>33.	Krebs P., Kurrer M.O., Kremer M., De Giuli R., Sonderegger I., Henke A., Maier R., Ludewig B. Molecular mapping of autoimmune B cell responses in experimental myocarditis. J. Autoimmun., 2007, vol. 28, no. 4, pp. 224–233.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>34.	Lacroix-Desmazes S., Moreau A., Sooryanarayana, Bonnemain C., Stieltjes N., Pashov A., Sultan Y., Hoebeke J., Kazatchkine M.D., Kaveri S.V. Catalytic activity of antibodies against factor VIII in patients with hemophilia A. Nat. Med., 1999, vol. 5, no. 9, pp. 1044–1047.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>35.	Lasky T., Terracciano G.J., Magder L., Koski C.L., Ballesteros M., Nash D., Clark S., Haber P., Stolley P.D., Schonberger L.B., Chen R.T. The Guillain–Barré syndrome and the 1992–1993 and 1993–1994 influenza vaccines. N. Engl. J. Med., 1998, vol. 339, no. 25, pp. 1797–1802.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>36.	Lawson C. Evidence for mimicry by viral antigens in animal models of autoimmune disease including myocarditis. Cell. Mol. Life. Sci., 2000, vol. 57, no. 4, pp. 552–560.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>37.	Li Z., Nardi M.A., Karpatkin S. Role of molecular mimicry to HIV-1 peptides in HIV-1-related immunologic thrombocytopenia. Blood, 2005, vol. 106, no. 2, pp. 572–576.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>38.	Liang B., Gardner D., Griswold D., Bugelski P., Song X.Anti-interleukin-6 monoclonal antibody inhibits autoimmune responses in a murine model of systemic lupus erythematosus. Immunology, 2006, vol. 119, no. 3, pp. 296–305.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>39.	Liu K., Iyoda T., Saternus M., Kimura Y., Inaba K., Steinman R.M. Immune tolerance after delivery of dying cells to dendritic cells in situ. J. Exp. Med., 2002, vol. 196, no. 8, pp. 1091–1097.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>40.	Mackay F., Silveira P.A., Brink R. B cells and the BAFF/APRIL axis: fast-forward on autoimmunity and signaling. Curr. Opin. Immunol., 2007, vol. 19, no. 3, pp. 327–336.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>41.	Martin D.A., Elkon K.B. Autoantibodies make a U-turn: the toll hypothesis for autoantibody specificity. J. Exp. Med., 2005, vol. 202, no. 11, pp. 1465–1469.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>42.	McNamara P., Flanagan B., Selby A., Hart C., Smyth R. Pro- and anti-inflammatory responses in respiratory syncytial virus bronchiolitis. Eur. Respir. J., 2004, vol. 23, no. 1, pp. 106–112.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>43.	Meite M., Leonard S., Idrissi M., Izui S., Masson P., Coutelier J. Exacerbation of autoantibody-mediated hemolytic anemia by viral infection. J. Virol., 2000, vol. 74, no. 13, pp. 6045–6049.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>44.	Mevorach D., Zhou J.L., Song X., Elkon K.B. Systemic exposure to irradiated apoptotic cells induces autoantibody production. J. Exp. Med., 1998, vol. 188, no. 2, pp. 387–392.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>45.	Moisini I., Davidson A. BAFF: a local and systemic target in autoimmune diseases. Clin. Exp. Immunol., 2009, vol. 158, no. 2, pp. 155–163.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>46.	Murawski M.R., Bowen G.N., Cerny A.M., Anderson L.J., Haynes L.M., Tripp R.A., Kurt-Jones E.A., Finberg R.W. Respiratory syncytial virus activates innate immunity through Toll-like receptor 2. J. Virol., 2009, vol. 83, no. 3, pp. 1492–1500.</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>47.	Nachamkin I., Shadomy S.V., Moran A.P., Cox N., Fitzgerald C., Ung H., Corcoran A.T., Iskander J.K., Schonberger L.B., Chen R.T. Anti-ganglioside antibody induction by swine (A/NJ/1976/H1N1) and other influenza vaccines: insights into vaccine-associated Guillain–Barré syndrome. J. Infect. Dis., 2008, vol. 198, no. 2, pp. 226–233.</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>48.	Orbach H., Agmon-Levin N., Zandman-Goddard G. Vaccines and autoimmune diseases of the adult. Discov. Med., 2010, vol. 9, no. 45, pp. 90–97.</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>49.	Paolieri F., Salmaso C., Battifora M., Montagna P., Pesce G., Bagnasco M., Richiusa P., Galluzzo A., Giordano C. Possible pathogenetic relevance of interleukin-1 beta in «destructive» organ-specific autoimmune disease (Hashimoto’s thyroiditis). Ann. N.Y. Acad. Sci., 1999, vol. 876, pp. 221–228.</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>50.	Pashov A., Kenderov A., Kyurkchiev S., Kehayov I., Hristova S., Lacroix-Desmazes S., Giltiay N., Varamballi S., Kazatchkine M., Kaveri S. Autoantibodies to heat shock protein 90 in the human natural antibody repertoire. Internat. Immunol., 2002, vol. 14, no. 5, pp. 453–461.</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>51.	Portocala R., Spyrou N., Lambropoulou V., Pateraki E. The presence of both antivirus and antiself antibodies in sera from patients with adenovirus and influenza B. Virologie, 1988, vol. 39, no. 3, pp. 207–216.</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>52.	Reed J.L., Welliver T.P., Sims G.P., McKinney L., Velozo L., Avendano L., Hintz K., Luma J., Coyle A.J., Welliver R.C. Innate immune signals modulate antiviral and polyreactive antibody responses during severe respiratory syncytial virus infection. J. Infect. Dis., 2009, vol. 199, no. 8, pp. 1128–1138.</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>53.	Richer M.J., Fang D., Shanina I., Horwitz M.S. Toll-like receptor 4-induced cytokine production circumvents protection conferred by TGF-beta in coxsackievirus-mediated autoimmune myocarditis. Clin. Immunol., 2006, vol. 121, no. 3, pp. 339–349.</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>54.	Saha S., Tieng A., Pepeljugoski K.P., Zandamn-Goddard G., Peeva E. Prolactin,systemic lupus erythematosus, and autoreactive B cells: lessons learnt from murine models. Clin. Rev. Allergy Immunol., 2011, vol. 40, no. 1, pp. 8–15.</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>55.	Roosnek E., Lanzavecchia A. Efficient and selective presentation of antigen-antibody complexes by rheumatoid factor B cells. J. Exp. Med., 1991, vol. 173, no. 2, pp. 487–489.</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>56.	Salonen E.M., Vaheri A., Suni J., Wager O. Rheumatoid factor in acute viral infections: interference with determination of IgM, IgG, and IgA antibodies in an enzyme immunoassay. J. Infect. Dis., 1980, vol. 142, no. 2, pp. 250–255.</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>57.	Sané F., Moumna I., Hober D. Group B coxsackieviruses and autoimmunity: focus on type 1 diabetes. Expert. Rev. Clin. Immunol., 2011, vol. 7, no. 3, pp. 357–366.</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>58.	Sangster M., Topham D., D’Costa S., Cardin R., Marion T., Myers L., Doherty P. Analysis of the virus-specific and nonspecific B cell response to a persistent B-lymphotropic gammaherpesvirus. J. Immunol., 2000, vol. 164, no. 4, pp. 1820–1828.</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>59.	Tzang B.S., Lee Y.J., Yang T.P., Tsay G.J., Shi J.Y., Tsai C.C., Hsu T.C. Induction of antiphospholipid antibodies and antiphospholipid syndrome-like autoimmunity in naive mice with antibody against human parvovirus B19 VP1 unique region protein. Clin. Chim. Acta, 2007, vol. 382, no. 1–2, pp. 31–36.</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>60.	Ulvestad E., Kanestrøm A., Tengnér P., Gjerde S., Sundal J., Haga H.J. Anti-cardiolipin autoantibodies and pulmonary embolism. A case for a common cause. Scand. J. Rheumatol., 2000, vol. 29, no. 5, pp. 330–333.</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>61.	Utz P.J., Anderson P. Posttranslational protein modifications, apoptosis, and the bypass of tolerance to autoantigens. Arthritis Rheum., 1998, vol. 41, no. 7, pp. 1152–1160.</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>62.	Zhang M., Carroll M.C. Natural IgM-mediated innate autoimmunity: a new target for early intervention of ischemia-reperfusion injury. Expert. Opin. Biol. Ther., 2007, vol. 7, no. 10, pp. 1575–1582.</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>63.	Zhen Q., Xie Ch., Wu T., Mackay M., Aranow C., Putterman C., Mohan Ch. Identification of autoantibody clusters that best predict lupus disease activity using glomerular proteome arrays. J. Clin. Invest., 2005, vol. 115, no. 12, pp. 3428–3439.</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>64.	Zhou Z.H., Tzioufas A.G., Notkins A.L. Properties and function of polyreactive antibodies and polyreactive antigen-binding B cells. J. Autoimmun., 2007, vol. 29, no. 4, pp. 219–228.</mixed-citation></ref></ref-list></back></article>
