Indian Journal of Dermatology
CORRESPONDENCE
Year
: 2021  |  Volume : 66  |  Issue : 2  |  Page : 196--198

Anti-neuronal IgG antibodies in bullous pemphigoid coexistent with neurodegeneration


Justyna Gornowicz-Porowska1, Agnieszka Seraszek-Jaros2, Monika Bowszyc-Dmochowska3, Paweł Bartkiewicz4, Elżbieta Kaczmarek2, Marian Dmochowski4,  
1 Department of Medicinal and Cosmetic Natural Products; Autoimmune Blistering Dermatoses Section, Department of Dermatology, Poznan University of Medical Sciences, Poznan, Poland
2 Department of Bioinformatics and Computational Biology, Poznan University of Medical Sciences, Poznan, Poland
3 Cutaneous Histopathology and Immunopathology Section, Department of Dermatology, Poznan University of Medical Sciences, Poznan, Poland
4 Autoimmune Blistering Dermatoses Section, Department of Dermatology, Poznan University of Medical Sciences, Poznan, Poland

Correspondence Address:
Justyna Gornowicz-Porowska
Department of Medicinal and Cosmetic Natural Products; Autoimmune Blistering Dermatoses Section, Department of Dermatology, Poznan University of Medical Sciences, Poznan
Poland




How to cite this article:
Gornowicz-Porowska J, Seraszek-Jaros A, Bowszyc-Dmochowska M, Bartkiewicz P, Kaczmarek E, Dmochowski M. Anti-neuronal IgG antibodies in bullous pemphigoid coexistent with neurodegeneration.Indian J Dermatol 2021;66:196-198


How to cite this URL:
Gornowicz-Porowska J, Seraszek-Jaros A, Bowszyc-Dmochowska M, Bartkiewicz P, Kaczmarek E, Dmochowski M. Anti-neuronal IgG antibodies in bullous pemphigoid coexistent with neurodegeneration. Indian J Dermatol [serial online] 2021 [cited 2021 Dec 6 ];66:196-198
Available from: https://www.e-ijd.org/text.asp?2021/66/2/196/313749


Full Text



Sir,

Previously, epidemiological data from a national registry indicated the association between bullous pemphigoid (BP) [Figure 1] and neurodegenerative disorders (ND).[1] BP antigens exist also in their neurological isoforms located in the central nervous system. Certain studies[2] directly linked ND and BP through an antibody-based mechanism.

We examined here, whether neural system antigens are recognized by the antibodies from BP patients as, to the best of our knowledge, there is a lack of data concerning the conceptual role of anti-neuronal antibodies underlying the risk of development of BP in ND patients.{Figure 1}

Thirty BP patients with the coincidence of ND (BP+ND) and 30 BP patients without the coincidence of ND (BP−ND) were investigated.

Sera were tested by immunoblotting using the Neuronal Antigens Profile Plus RST kit (Euroimmun, Luebeck, Germany) for antibodies to the panel of individual neuronal antigens [Figure 2], whereas antibodies to BP180/BP230 were detected with commercially available enzyme-linked immunosorbent assays (ELISAs) (Euroimmun, Luebeck, Germany). Statistical analyses were performed using statistical analysis Software Statistica PL 10.0 (StatSoft Inc.).{Figure 2}

Negative correlations were found in BP + ND patients between the presence of anti-BP180 IgG and anti-Yo IgG antibodies (r = −0.430, P = 0.0318) and in BP − ND patients between the presence of anti-BP180 IgG and anti-CRMP-5 IgG antibodies (r = −0.402, P = 0.0308).

The percentage of the occurrence of examined anti-neuronal antibodies in both groups (BP+ND, BP−ND) is presented in [Table 1].{Table 1}

Fisher's exact test revealed a lack of association between reactivity against any antigens that are present in the immunoblot in examined groups (BP + ND and BP − ND; P = 1.000).

Our findings gently suggest that PNMA2 in patients with ND may be a herald of BP, however, further investigations with a larger population and longer follow-up are needed. The observations reported here may indicate the immunogenetic mechanisms involved in the association between ND and BP. Messingham et al.[3] suggested that the initial loss of tolerance to neuronal BP180 may contribute to the risk of subsequent development of cutaneous BP. It is also postulated that the HLA-DQB1*03:01 allele, with a well-established role in susceptibility to the pemphigoids, may serve as an additional link between ND and BP, catalyzing the process of epitope spreading from neuronal BP180 to hemidesmosomal BP180 or vice versa.[4] In addition, a possible genetic background of ND and BP may also be related to the chromosomal assignment.

There is no relationship between IgG antibodies to BP180/BP230 and IgG anti-neuronal antibodies in BP+ND. Nevertheless, it is speculated that PNMA2-collagen interactions in certain patients might be associated with the coexistence of BP with ND irrespective of malignancy suggesting the necessity of holistic treatment strategies.

Acknowledgments

A part of this study was presented at the International Investigative Dermatology (IID) 2018 Meeting, 16–19 May 2018, Orlando, Florida, USA and published as an abstract #256: Dmochowski M, Gornowicz-Porowska J, Bartkiewicz P, Seraszek-Jaros A, Kaczmarek E, Bowszyc-Dmochowska M.: Comparative analysis of occurrence of IgG antibodies to BP180/BP230 and so-called IgG anti-neuronal antibodies in BP coexistent with neurodegenerative diseases, J Invest Dermatol (2018), 138(5S), supplement 1:S44.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

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