<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JIBTVA</journal-id><journal-title-group><journal-title>Journal of Immune Based Therapies, Vaccines and Antimicrobials</journal-title></journal-title-group><issn pub-type="epub">2168-1546</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jibtva.2014.32004</article-id><article-id pub-id-type="publisher-id">JIBTVA-44945</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Additional Treatment Modality to Improve Outcomes in Myocardial Infarctions and Strokes
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>imon</surname><given-names>Skurkovich</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Boris</surname><given-names>Skurkovich</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Warren Alpert Medical School of Brown University, Providence, USA</addr-line></aff><aff id="aff1"><addr-line>Advanced Biotherapy Laboratories, Rockville, USA</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>sskurkovich@gmail.com(IS)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>26</day><month>03</month><year>2014</year></pub-date><volume>03</volume><issue>02</issue><fpage>29</fpage><lpage>31</lpage><history><date date-type="received"><day>31</day>	<month>March</month>	<year>2014</year></date><date date-type="rev-recd"><day>10</day>	<month>April</month>	<year>2014</year>	</date><date date-type="accepted"><day>17</day>	<month>April</month>	<year>2014</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  
    In 1974, in Nature, we hypothesized that removal of cytokines can be effective in the treatment of certain inflammatory diseases, e.g., rheumatoid arthritis (RA). We call this approach anticytokino-therapy. Later it was shown that neutralization of pro-inflammatory cytokines, such as tumor necrosis factor alpha (TNF-α), interferon alpha (IFN-α), interferon gamma (IFN-γ), and interleukin 6 (IL-6), leads to a good therapeutic effect. Anticytokinotherapy is currently used around the world for the treatment of rheumatoid arthritis, psoriasis, psoriatic arthritis, and other Th-1-mediated inflammatory diseases. Pro-inflammatory cytokines have also been found in other conditions (myocardial infarctions, strokes, chronic pain syndromes, etc.). This leads us to believe that hyper- production of pro-inflammatory cytokines forms a basis of a variety of pathological conditions and represents a uniform response of the organism to a wide variety of insults in any part of the body. Thus, we propose to add monoclonal antibodies to (or other blockers of) pro-inflammatory cytokines to the treatment regimens for myocardial infarctions, strokes, and possibly other Th-1-mediated diseases. 
  
 
</p></abstract><kwd-group><kwd>Neutralization of Pro-Inflammatory Cytokines</kwd><kwd> Myocardial Infarction</kwd><kwd> Stroke</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>References</title></sec><sec id="s2"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.44945-ref1"><label>1</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Skurkovich</surname><given-names> S.V.</given-names></name>,<name name-style="western"><surname> Klinova</surname><given-names> E.G.</given-names></name>,<name name-style="western"><surname> Aleksandrovskaya</surname><given-names> I.M.</given-names></name>,<name name-style="western"><surname> Levina</surname><given-names> N.V.</given-names></name>,<name name-style="western"><surname> Arkhipova</surname><given-names> N.A. and Bulicheva</given-names></name>,<name name-style="western"><surname> T.I. </surname><given-names>  </given-names></name>,<etal>et al</etal>. (<year>1973</year>)<article-title>Stimulation of Transplantation Immunity and Plasma Cell Reaction by Interferon in Mice</article-title><source> Immunology</source><volume> 25</volume>,<fpage> 317</fpage>-<lpage>322</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.44945-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Skurkovich, S.V., Klinova, E.G., Eremkina, E.I. and Levina, N.V. (1974) Immunosuppressive Effect of an Anti-Interferon Serum. Nature, 247, 551-552.http://dx.doi.org/10.1038/247551a0</mixed-citation></ref><ref id="scirp.44945-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Skurkovich, S. and Skurkovich, B. (1989) The Development of Autoimmune Diseases is Connected with the Initial Disturbance of Interferon Synthesis in the Cells. Journal of Interferon Research, 9, S305.</mixed-citation></ref><ref id="scirp.44945-ref4"><label>4</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Skurkovich</surname><given-names> S.V.</given-names></name>,<name name-style="western"><surname> Loukina</surname><given-names> G.V.</given-names></name>,<name name-style="western"><surname> Sigidin</surname><given-names> Y.A. and Skurkovich</given-names></name>,<name name-style="western"><surname> B. </surname><given-names>  </given-names></name>,<etal>et al</etal>. (<year>1998</year>)<article-title>Successful First-Time Use of Antibodies to Interferon-Gamma Alone and Combined with Antibodies to Tumor Necrosis Factor Alpha to Treat Rheumatic Diseases (Rheumatoid Arthritis, Systemic Lupus Erythemotosus, Psoriatic Arthritis, Behcet’s Syndrome)</article-title><source> Intern Journal of Immunotherapy</source><volume> 14</volume>,<fpage> 23</fpage>-<lpage>32</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.44945-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Elliott, M.J., Maini, R.N., Feldmann, M., Kalden, J.R., Antoni, C., Smolen, J.S., Leeb, B., Breedveld, F.C., Macfarlane, J.D., Bijl, H. and Woody, J.N. (1994) Randomized Double-Blind Comparison of Chimeric Monoclonal Antibody to Tumor Necrosis Factor Alpha (cA2) versus Placebo in Rheumatoid Arthritis. Lancet, 344, 1105-1110.http://dx.doi.org/10.1016/S0140-6736(94)90628-9</mixed-citation></ref><ref id="scirp.44945-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Skurkovich, B. and Skurkovich, S. (2006) Inhibition of IFN-as a Method of Treatment of Various Autoimmune Diseases, Including Skin Diseases. Ernst Schering Res Found Workshop, 56, 1-27.  
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