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Case Report
Importance of Measures against
Staphylococcus aureus in Atopic
Dermatitis as a Superantigen Disease -
Kazuo Sugimoto1
*, Takamichi Hattori2
, Yoshio Kitsukawa3
, Akiyo
Aotsuka3
, Takeshi Wada3
, Hitoshi Kubosawa4
and Shoichi Ito5
1
Department of Clinical Allergology, Neurology Clinic Tsudanuma, Japan
2
Department of Neurology, Neurology Clinic Tsudanuma, Japan
3
Internal Medicine, Chiba Aoba Municipal Hospital, Japan
4
Clinical Pathology, Chiba Aoba Municipal Hospital, Japan
5
Department of Neurology, Chiba University Graduate School of Medicine, Japan
*Address for Correspondence: Kazuo Sugimoto, Department of Clinical Allergology, Neurology
Clinic Tsudanuma, Japan, E-mail: ka.sugimoto.chiba.jp@nifty.com
Submitted: 13 November 2016; Approved: 01 March 2017; Published: 04 March 2017
Citation this article: Sugimoto K, Hattori T, Kitsukawa Y, Aotsuka A, Wada T, et al. Importance of
Measures against Staphylococcus aureus in Atopic Dermatitis as a Superantigen Disease. Sci J Clin
Res Dermatol. 2017;2(1): 007-009.
Copyright: © 2017 Sugimoto K, et al. This is an open access article distributed under the Creative
Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any
medium, provided the original work is properly cited.
Scientific Journal of
Clinical Research in Dermatology
SCIRES Literature - Volume 2 Issue 1 - www.scireslit.com Page - 008
Scientific Journal of Clinical Research in Dermatology
BACKGROUND
There are reports that Staphylococcus aureus (S. aureus) is
involved in the onset and exacerbation of Atopic Dermatitis (AD)
[1]. In the United States bleach bath therapy is incorporated into the
guidelines for treatment of AD. For these reasons, measures against
S. aureus in AD are important. In addition to skin, Yamada et al. [2]
reported inflammation of intestinal tract for patients with AD, and
Kira et al. [3] reported inflammation of the cervical vertebrae. Kino
et al. [4] reported inflammation in the colon of infants with AD. Ito
et al. [5] reported the neurologic findings and Magnetic Resonance
Imaging (MRI) of patients with AD; they concluded that AD might
become the risk factor in disc degeneration. IgE antibody titer to the
toxin which is produced by S. aureus is able to reflect the pathogenesis
of AD as shown in a number of reports[6-9].
METHOD
In addition to the conventional treatment with topical steroids
and moisturizing agents for AD patients the researchers treated
S. aureus using disinfectants, such as Isodine®
solution [10]. As a
result, short term improvements in patients’ skin rash were seen. For
patients who wish to be examined among AD patients, patients with
abnormalities such as neurological reflex were further examined for
MRI of the cervical vertebrae. In addition, endoscopic examination
including duodenal biopsy was performed for those who wanted
examination among patients with AD. Detection of toxins produced
by S. aureus was also examined by Polymerase Chain Reaction (PCR)
method in S. aureus specimens detected from rashes of patients with
AD. We also examined IgE antibodies to Staphylococcal Enterotoxins
A (SEA) and Staphylococcal Enterotoxins B (SEB) of AD patients
over time.
RESULTS
Regarding the neurological abnormalities that are sometimes
seen in patients with AD, we identified neurological abnormalities in
89 patients of 110 AD patients (80.9%). Using MRI, we also observed
an abnormality in the cervical spine of 54 patients of 69 AD patients
(78.2%) who showed a neurological abnormality.
We have observed 21 patients of the 32 AD patients (65.6%) in
the damage of both the duodenum and the cervical spine. We also
observedduodenitisin43of53duodenal-biopsiedADpatients.Along
with the improvement of the rash by Staphylococcal disinfection skin
care method for AD that we have developed[10], of 12 patients with
repeated duodenum biopsies, the duodenitis had normalized in five
cases [11]. We have already reported detection rate of toxin using PCR
from S. aureus, which is detected from patients with AD who visited
our hospital. The detection rates of staphylococcal enterotoxins A, B,
C and E were 9.7, 55.6, 7.7 and 30.6%, respectively. The detection rate
of toxic shock syndrome toxin 1 was 6.6% and those of exfoliative
toxins A and B were 4.1 and 1.5%. The total detection rate of toxins
was 80.1% from 196 S. aureus strains [11].
DISCUSSION
We developed a treatment regimen that uses a disinfectant against
S. aureus detected from the skin of a patient with AD as a general
treatment for the treatment of AD; we have reported some effects
[10-13]. There is also a report that S. aureus is involved in the onset
and exacerbation of AD[1]. In the United States bleach bath therapy
is incorporated into the guidelines for treatment of AD. For these
reasons, measures against S. aureus in AD are important. S. aureus
produces toxins at a high rate. Produced toxin acts as a Superantigen
[15] to humans. Ochi et al. [16] reported that superantigen is involved
in disorders of the cervical spine. In patients with AD, many disorders
of the intestinal tract and cervical vertebrae are found in addition to
the skin. In the same patient with AD, there were many cases in which
disorder of the intestinal tract and cervical vertebrae was observed in
addition to the skin, and the frequency was high, and we experienced
cases where the disorder became normal when worried by treatment.
We also experienced a number of cases in which treatment with IgE
antibodies to SEA and SEB of patients with AD improves over time by
treatment [6-9]. Last year, authors had reported for the first time in
the world that AD may be one of the Superantigen Diseases [17]. The
Journal of Pharmaceutical Microbiology titled Staphylococcus aureus
vs. AD published in April 2016 was published[18].
CONCLUSION
Lesions of patients with atopic dermatitis were not only in the
skin but also in the intestinal tract and the cervical vertebrae with
high - frequency disorder. A high rate of S. aureus is detected from
rash in patients with AD. S. aureus produces toxins. The detection
rate of toxin produced by S. aureus is high, and toxin acts on people
as superantigens. IgE antibodies to SEA and SEB are improved by
improvement of the eruption. For these reasons, AD was proposed
as the world’s first super-antigenic disease last year [17]. From now
on, it seems indispensable to introduce a treatment which takes wide
countermeasures against S. aureus in the treatment of AD [10-14,17-
19].
REFERENCES
1. Kobayashi T, Glatz M, Horiuchi K, Kawasaki H, Akiyama H, Kaplan DH, et
al. Dysbiosis and Staphylococcus aureus Colonization Drives Inflammation in
Atopic Dermatitis. Immunity. 2015; 42: 756-66. https://goo.gl/CHqMGG
2. Yamada H, Izutani R, Chihara J, Yudate T, Matsukura M, Tezuka T. RANTES
mRNA expression in skin and colon of patients with atopic dermatitis. Int Arch
Allergy Immunol. 1996; 111(suppl 1): 19-21. https://goo.gl/0iGLWR
3. Kira J, Yamasaki K, Kawano Y, Kobayashi T Acute myelitis associated
with hyperIgEemia and atopic dermatitis. Neurol Sci. 1997; 148: 199-203.
https://goo.gl/QRR7eG
4. Kino M, Kojima T, Yamamoto A, Sasal M, Taniuchi S, Kobayashi Y. Bowel
ABSTRACT
Patients with AD showed high incidence of duodenitis and cervical spine as a disorder other than skin. We experienced many cases
where treatment resulted in improvement of eruptions of AD and other disorders other than skin were alleviated. We also experienced
patients with AD with duodenitis normalized by repeated testing. In the same case of AD, many disorders of the organs of the duodenum
and the cervical spine were observed. The toxin produced by S. aureus detected from the skin of patients with AD was high rate.
Keywords: Atopic dermatitis; Staphylococcus aureus; Superantigen; Disinfectant; IgE antibodies to SEA and SEB
SCIRES Literature - Volume 2 Issue 1 - www.scireslit.com Page - 009
Scientific Journal of Clinical Research in Dermatology
wall thickening in infants with food allergy. Pediatr Radiol. 2002; 32: 31-3.
https://goo.gl/SXPw0y
5. Ito S, Hattori T, Fukutake T, Sugimoto K. Is atopic dermatitis a risk factor
for intervertebral disc degeneration? A preliminary clinical and MRI study. J
Neurol Sci. 2003; 206: 39-42. https://goo.gl/35dlAC
6. Bunikowski R, Mielke M, Skarabis H, Herz U, Bergmann RL, Wahn U, et al.
Prevalence and role of serum IgE antibodies to the Staphylococcus aureus
- derived Superantigens SEA and SEB in children with atopic dermatitis. J
Allergy Clin Immunol. 1999; 103: 119-24. https://goo.gl/LLgkrf
7. Nomura I, Tanaka K, Tomita H, Katsunuma T, Ohya Y, Ikeda N, et al.
Evaluation of the staphylococcal exotoxins and their specific IgE in
childhood atopic dermatitis. J Allergy Clin Immunol. 1999; 104: 441-6.
https://goo.gl/loDydK
8. Tada J, Toi Y, Akiyama H, Arata J, Kato H. Presence of specific IgE antiodies
to staphylococcal enterotoxins in patients with atopic dermatitis. Eur J
Dermatol. 1996; 6: 552-4.
9. Bunikowski R, Mielke ME, Skarabis H, Worm M, Anagnostopoulos I, Kolde
G, et al. Evidence for a disease - promoting effect of Staphylococcus aureus
- derived exotoxins in atopic dermatitis. J Allergy Clin Immunol. 2000; 105:
814-9. https://goo.gl/XnePhP
10. Sugimoto K, Kuroki H, Kanazawa M, Kurosaki T, Abe H, Takahashi Y, et al.
New successful treatment with disinfectant for atopic dermatitis. Dermatol.
1997; 195: 62-8. https://goo.gl/ERu1aH
11. Sugimoto K, Ishikawa N, Terano T, Kitukawa Y, Kubosawa H, Ito S, et al. The
importance of Bacterial superantigens Produced by Staphylococcus aureus
in the Treatment of Atopic Dermatitis Using Povidone-Iodine. Dermatology.
2006; 212: 26-34. https://goo.gl/u5nBAv
12. Sugimoto K, Ishikawa N, Sugioka T, Nakamura M, Koneki H, et al. (1998)
Isojin® disinfectant therapy for atopic dermatitis. Japanese J Pediatric
Dermatol. 17: 103-7.
13. Sugimoto K, Ishikawa N, Ogawa A (1998) Treatment of Staphylococcus
aureus by disinfection treatment of patients with atopic dermatitis. Hifu. 40:
117-24.
14. Sugimoto K, Ishikawa N, Sugioka T, Koseki H, Kubosawa H, Kagawa S, et
al. The importance of disinfection therapy using povidone-iodine solution in
atopic dermatitis. Dermatology. 2002; 204: 63-9. https://goo.gl/Zk9eW2
15. White J, Herman A, Pullen AM, Kubo R, K appler JW, Marrack P. The V
beta-specific super antigen staphylococcal enterotoxin B: stimulation of
mature T cells and clonal detection in neonatal mice. Cell. 1989; 56: 27-35.
https://goo.gl/5AcrHv
16. Ochi H, Osoegawa M, Murai H, Minohara M, Taniwaki T, Kira J. Presence
of IgE Antibodies to Bacterial superantigens and Increased IL-13-Producing
T Cells in Myelitic Patients with Atopic Diathesis. In Arch Allergy Immunol.
2004; 134: 41-8. https://goo.gl/OyHGN1
17. Sugimoto K, Kitukawa Y, Aotsuka A, Wada T, Kubosawa H, et al. Is Atopic
Dermatitis One of the superantigens Diseases? J Dermatolog Clin Res. 2015;
3: 1052-3. https://goo.gl/95X4G6
18. Sugimoto K. Staphylococcus-aureus-vs-Atopic-Dermatitis. J Pharm Microbiol.
2016; 2: 8:1-3. https://goo.gl/1GtKIz
19. Sugimoto K, Hattori T, Kitukawa Y, Aotsuka A, Wada T, et al. The Treatment
of Symptoms in Atopic Dermatitis as a Superantigen Disease. Journal of
Microbiology and Modern Techniques. 2016; 1: 1-3. https://goo.gl/5rcTG4

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Scientifi c Journal of Clinical Research in Dermatology

  • 1. Case Report Importance of Measures against Staphylococcus aureus in Atopic Dermatitis as a Superantigen Disease - Kazuo Sugimoto1 *, Takamichi Hattori2 , Yoshio Kitsukawa3 , Akiyo Aotsuka3 , Takeshi Wada3 , Hitoshi Kubosawa4 and Shoichi Ito5 1 Department of Clinical Allergology, Neurology Clinic Tsudanuma, Japan 2 Department of Neurology, Neurology Clinic Tsudanuma, Japan 3 Internal Medicine, Chiba Aoba Municipal Hospital, Japan 4 Clinical Pathology, Chiba Aoba Municipal Hospital, Japan 5 Department of Neurology, Chiba University Graduate School of Medicine, Japan *Address for Correspondence: Kazuo Sugimoto, Department of Clinical Allergology, Neurology Clinic Tsudanuma, Japan, E-mail: ka.sugimoto.chiba.jp@nifty.com Submitted: 13 November 2016; Approved: 01 March 2017; Published: 04 March 2017 Citation this article: Sugimoto K, Hattori T, Kitsukawa Y, Aotsuka A, Wada T, et al. Importance of Measures against Staphylococcus aureus in Atopic Dermatitis as a Superantigen Disease. Sci J Clin Res Dermatol. 2017;2(1): 007-009. Copyright: © 2017 Sugimoto K, et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Scientific Journal of Clinical Research in Dermatology
  • 2. SCIRES Literature - Volume 2 Issue 1 - www.scireslit.com Page - 008 Scientific Journal of Clinical Research in Dermatology BACKGROUND There are reports that Staphylococcus aureus (S. aureus) is involved in the onset and exacerbation of Atopic Dermatitis (AD) [1]. In the United States bleach bath therapy is incorporated into the guidelines for treatment of AD. For these reasons, measures against S. aureus in AD are important. In addition to skin, Yamada et al. [2] reported inflammation of intestinal tract for patients with AD, and Kira et al. [3] reported inflammation of the cervical vertebrae. Kino et al. [4] reported inflammation in the colon of infants with AD. Ito et al. [5] reported the neurologic findings and Magnetic Resonance Imaging (MRI) of patients with AD; they concluded that AD might become the risk factor in disc degeneration. IgE antibody titer to the toxin which is produced by S. aureus is able to reflect the pathogenesis of AD as shown in a number of reports[6-9]. METHOD In addition to the conventional treatment with topical steroids and moisturizing agents for AD patients the researchers treated S. aureus using disinfectants, such as Isodine® solution [10]. As a result, short term improvements in patients’ skin rash were seen. For patients who wish to be examined among AD patients, patients with abnormalities such as neurological reflex were further examined for MRI of the cervical vertebrae. In addition, endoscopic examination including duodenal biopsy was performed for those who wanted examination among patients with AD. Detection of toxins produced by S. aureus was also examined by Polymerase Chain Reaction (PCR) method in S. aureus specimens detected from rashes of patients with AD. We also examined IgE antibodies to Staphylococcal Enterotoxins A (SEA) and Staphylococcal Enterotoxins B (SEB) of AD patients over time. RESULTS Regarding the neurological abnormalities that are sometimes seen in patients with AD, we identified neurological abnormalities in 89 patients of 110 AD patients (80.9%). Using MRI, we also observed an abnormality in the cervical spine of 54 patients of 69 AD patients (78.2%) who showed a neurological abnormality. We have observed 21 patients of the 32 AD patients (65.6%) in the damage of both the duodenum and the cervical spine. We also observedduodenitisin43of53duodenal-biopsiedADpatients.Along with the improvement of the rash by Staphylococcal disinfection skin care method for AD that we have developed[10], of 12 patients with repeated duodenum biopsies, the duodenitis had normalized in five cases [11]. We have already reported detection rate of toxin using PCR from S. aureus, which is detected from patients with AD who visited our hospital. The detection rates of staphylococcal enterotoxins A, B, C and E were 9.7, 55.6, 7.7 and 30.6%, respectively. The detection rate of toxic shock syndrome toxin 1 was 6.6% and those of exfoliative toxins A and B were 4.1 and 1.5%. The total detection rate of toxins was 80.1% from 196 S. aureus strains [11]. DISCUSSION We developed a treatment regimen that uses a disinfectant against S. aureus detected from the skin of a patient with AD as a general treatment for the treatment of AD; we have reported some effects [10-13]. There is also a report that S. aureus is involved in the onset and exacerbation of AD[1]. In the United States bleach bath therapy is incorporated into the guidelines for treatment of AD. For these reasons, measures against S. aureus in AD are important. S. aureus produces toxins at a high rate. Produced toxin acts as a Superantigen [15] to humans. Ochi et al. [16] reported that superantigen is involved in disorders of the cervical spine. In patients with AD, many disorders of the intestinal tract and cervical vertebrae are found in addition to the skin. In the same patient with AD, there were many cases in which disorder of the intestinal tract and cervical vertebrae was observed in addition to the skin, and the frequency was high, and we experienced cases where the disorder became normal when worried by treatment. We also experienced a number of cases in which treatment with IgE antibodies to SEA and SEB of patients with AD improves over time by treatment [6-9]. Last year, authors had reported for the first time in the world that AD may be one of the Superantigen Diseases [17]. The Journal of Pharmaceutical Microbiology titled Staphylococcus aureus vs. AD published in April 2016 was published[18]. CONCLUSION Lesions of patients with atopic dermatitis were not only in the skin but also in the intestinal tract and the cervical vertebrae with high - frequency disorder. A high rate of S. aureus is detected from rash in patients with AD. S. aureus produces toxins. The detection rate of toxin produced by S. aureus is high, and toxin acts on people as superantigens. IgE antibodies to SEA and SEB are improved by improvement of the eruption. For these reasons, AD was proposed as the world’s first super-antigenic disease last year [17]. From now on, it seems indispensable to introduce a treatment which takes wide countermeasures against S. aureus in the treatment of AD [10-14,17- 19]. REFERENCES 1. Kobayashi T, Glatz M, Horiuchi K, Kawasaki H, Akiyama H, Kaplan DH, et al. Dysbiosis and Staphylococcus aureus Colonization Drives Inflammation in Atopic Dermatitis. Immunity. 2015; 42: 756-66. https://goo.gl/CHqMGG 2. Yamada H, Izutani R, Chihara J, Yudate T, Matsukura M, Tezuka T. RANTES mRNA expression in skin and colon of patients with atopic dermatitis. Int Arch Allergy Immunol. 1996; 111(suppl 1): 19-21. https://goo.gl/0iGLWR 3. Kira J, Yamasaki K, Kawano Y, Kobayashi T Acute myelitis associated with hyperIgEemia and atopic dermatitis. Neurol Sci. 1997; 148: 199-203. https://goo.gl/QRR7eG 4. Kino M, Kojima T, Yamamoto A, Sasal M, Taniuchi S, Kobayashi Y. Bowel ABSTRACT Patients with AD showed high incidence of duodenitis and cervical spine as a disorder other than skin. We experienced many cases where treatment resulted in improvement of eruptions of AD and other disorders other than skin were alleviated. We also experienced patients with AD with duodenitis normalized by repeated testing. In the same case of AD, many disorders of the organs of the duodenum and the cervical spine were observed. The toxin produced by S. aureus detected from the skin of patients with AD was high rate. Keywords: Atopic dermatitis; Staphylococcus aureus; Superantigen; Disinfectant; IgE antibodies to SEA and SEB
  • 3. SCIRES Literature - Volume 2 Issue 1 - www.scireslit.com Page - 009 Scientific Journal of Clinical Research in Dermatology wall thickening in infants with food allergy. Pediatr Radiol. 2002; 32: 31-3. https://goo.gl/SXPw0y 5. Ito S, Hattori T, Fukutake T, Sugimoto K. Is atopic dermatitis a risk factor for intervertebral disc degeneration? A preliminary clinical and MRI study. J Neurol Sci. 2003; 206: 39-42. https://goo.gl/35dlAC 6. Bunikowski R, Mielke M, Skarabis H, Herz U, Bergmann RL, Wahn U, et al. Prevalence and role of serum IgE antibodies to the Staphylococcus aureus - derived Superantigens SEA and SEB in children with atopic dermatitis. J Allergy Clin Immunol. 1999; 103: 119-24. https://goo.gl/LLgkrf 7. Nomura I, Tanaka K, Tomita H, Katsunuma T, Ohya Y, Ikeda N, et al. Evaluation of the staphylococcal exotoxins and their specific IgE in childhood atopic dermatitis. J Allergy Clin Immunol. 1999; 104: 441-6. https://goo.gl/loDydK 8. Tada J, Toi Y, Akiyama H, Arata J, Kato H. Presence of specific IgE antiodies to staphylococcal enterotoxins in patients with atopic dermatitis. Eur J Dermatol. 1996; 6: 552-4. 9. Bunikowski R, Mielke ME, Skarabis H, Worm M, Anagnostopoulos I, Kolde G, et al. Evidence for a disease - promoting effect of Staphylococcus aureus - derived exotoxins in atopic dermatitis. J Allergy Clin Immunol. 2000; 105: 814-9. https://goo.gl/XnePhP 10. Sugimoto K, Kuroki H, Kanazawa M, Kurosaki T, Abe H, Takahashi Y, et al. New successful treatment with disinfectant for atopic dermatitis. Dermatol. 1997; 195: 62-8. https://goo.gl/ERu1aH 11. Sugimoto K, Ishikawa N, Terano T, Kitukawa Y, Kubosawa H, Ito S, et al. The importance of Bacterial superantigens Produced by Staphylococcus aureus in the Treatment of Atopic Dermatitis Using Povidone-Iodine. Dermatology. 2006; 212: 26-34. https://goo.gl/u5nBAv 12. Sugimoto K, Ishikawa N, Sugioka T, Nakamura M, Koneki H, et al. (1998) Isojin® disinfectant therapy for atopic dermatitis. Japanese J Pediatric Dermatol. 17: 103-7. 13. Sugimoto K, Ishikawa N, Ogawa A (1998) Treatment of Staphylococcus aureus by disinfection treatment of patients with atopic dermatitis. Hifu. 40: 117-24. 14. Sugimoto K, Ishikawa N, Sugioka T, Koseki H, Kubosawa H, Kagawa S, et al. The importance of disinfection therapy using povidone-iodine solution in atopic dermatitis. Dermatology. 2002; 204: 63-9. https://goo.gl/Zk9eW2 15. White J, Herman A, Pullen AM, Kubo R, K appler JW, Marrack P. The V beta-specific super antigen staphylococcal enterotoxin B: stimulation of mature T cells and clonal detection in neonatal mice. Cell. 1989; 56: 27-35. https://goo.gl/5AcrHv 16. Ochi H, Osoegawa M, Murai H, Minohara M, Taniwaki T, Kira J. Presence of IgE Antibodies to Bacterial superantigens and Increased IL-13-Producing T Cells in Myelitic Patients with Atopic Diathesis. In Arch Allergy Immunol. 2004; 134: 41-8. https://goo.gl/OyHGN1 17. Sugimoto K, Kitukawa Y, Aotsuka A, Wada T, Kubosawa H, et al. Is Atopic Dermatitis One of the superantigens Diseases? J Dermatolog Clin Res. 2015; 3: 1052-3. https://goo.gl/95X4G6 18. Sugimoto K. Staphylococcus-aureus-vs-Atopic-Dermatitis. J Pharm Microbiol. 2016; 2: 8:1-3. https://goo.gl/1GtKIz 19. Sugimoto K, Hattori T, Kitukawa Y, Aotsuka A, Wada T, et al. The Treatment of Symptoms in Atopic Dermatitis as a Superantigen Disease. Journal of Microbiology and Modern Techniques. 2016; 1: 1-3. https://goo.gl/5rcTG4