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Autoimmune Blistering Disease- Diagnostic Methodology for Pemphigus and Pemphigoid -
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EBABP
Epidermal side
Dermal side
Epidermal side
Dermal side
Dsg3
Dsg1
Epidermal cell-cell junction
ComplementNC16a
Blister
Anti-BP230
Anti-BP180
Blister
Anti-type VII collagen
Anchoring fibril
BP230
BP180
BP230BP230
BP180BP180
Anchoring fibril
BP230
BP180
Pemphigus
Structure of the epidermis
The epidermis generally consists of four layers: basal
layer (stratum basale), spinous layer (stratum spinosum),
granular layer (stratum granulosum), and cornified layer
(stratum corneum). Keratinocytes are the major component
of the epidermis. These cells progressively differentiate
from basal cells to the finally differentiated, cornified
layer, the outermost layer of the epidermis. Several
types of intercellular junctions in the epidermis, such as
desmosomes and tight junctions, are involved in protection
against mechanical stress, physical stimulation or infectious
agents. Desmosomes are composed of transmembrane
proteins [e.g., desmoglein (Dsg) 1, Dsg3, and desmocollin]
and intracellular proteins (e.g., desmoplakin). Desmogleins
and desmocollins, which are the cadherin family proteins,
maintain epidermal cohesion in a Ca2+-dependent manner.
Basal layer, the deepest layer of the epidermis, rests
upon the basement membrane zone (BMZ) of dermal-
epidermal junction (DEJ). Keratinocytes in basal layers
have hemidesmosome, a structure comparable to a half
of desmosome, being involved in adhesion in DEJ. Two
hemidesmosomal components, BP180 [BPAG2 (bullous
pemphigoid antigen 2), or type XVII collagen] and
integrin α6β4 are transmembrane proteins which link to
BMZ. BP230 (BPAG1) and plectin (HD-1) are cytoplasmic
proteins involved in the organization of the cytoskeleton.
BMZ is divided into the lamina densa and the lamina lucida.
The major component of the lamina densa is type IV
collagen. The lamina lucida contains heparan sulfate
proteoglycan, fibronectin and Laminin 332 (laminin 5).
Laminin 332 serves as a major anchoring protein between
the lamina lucida and the lamina densa and connects
BP180 and integrin α6β4 in the lamina lucida with type VII
collagen. Type VII collagen secures the lamina densa to the
dermis through association with dermis collagens.
Blistering disease is the general term for several diseases
with blisters and erosion on the skin and mucous membrane
caused by congenital or acquired interruptions of
epidermal or epidermal-dermal cohesions. 1-3) This
brochure summarizes the clinical manifestations, the
mechanism of the blister formation, and the serological
diagnosis on various autoimmune blistering diseases.
Cornified layer
Spinous layer
Granular layer
Basal layer
Epidermis
Basement membrane zone
Integrin α6β4
Dermis collagen
BP230BP230Plectin
Anchoring fibril(Type VII collagen)Anchoring fibril(Type VII collagen)
Desmocollin
Dsg3: desmoglein 3
Dsg1: desmoglein 1
Desmocollin
Dsg3: desmoglein 3
Dsg1: desmoglein 1
Laminin 332
Plakoglobin
Plakophilin
Desmoplakin
Epidermal cells
Epidermal cells
Epidermal cells
Epidermal cells
Basal cellsBasal cells
Lamina lucida
Lamina densa
Lamina lucida
Lamina densa
Dermis
DermisDermis
Desmosome
Hemi-desmosome
Desmosome
Hemi-desmosome
Basement membrane zoneBasement membrane zone
BP180BP180
Pemphigusgroup
Pemphigoidgroup
Pemphigus vulgaris, PV
Paraneoplastic pemphigus, PNP
Herpetiform pemphigus
Drug-induced pemphigus
Neonatal pemphigus
IgA pemphigus (Intraepidermal neutrophilic IgA dermatosis)
Bullous pemphigoid, BP Epidermolysis bullosa acquisita, EBA
Mucous membrane pemphigoid, MMP Dermatitis herpetiformis [Dühring]
Linear IgA bullous dermatosis, LAD Anti-p200 pemphigoid(Anti-laminin γ1 pemphigoid)
Pemphigus foliaceus, PF
Pemphigus erythematosus (PF localized type)
Brazilian pemphigus (PF endemic type)
Herpes gestationis, HG (BP subtype)
Pemphigus vegetans (PV subtype)
Mucosal dominant type
Mucocutaneous type
Others
Classification of autoimmune blistering diseases
Normal skin Epidermal cell-cell junction
Dermal-epidermal junction
3Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid -
Structure of the epidermis
Classification of autoimmune blistering diseases 3
Pemphigus
Clinical characterization 4
Pemphigus (PV/PF) and anti-desmoglein 1 & 3 IgG autoantibodies 5
Pemphigoid
Clinical characterization 6
Salt-split skin immunofluorescence 7
Bullous pemphigoid (BP) and anti-BP180 and anti-BP230 IgG autoantibodies 8
Epidermolysis bullosa acquisita (EBA) and anti-type VII collagen IgG autoantibodies 8
Sites of the skin blister formation in BP and EBA 8
ELISA kits for the diagnosis of autoimmune blistering diseases
Differential diagnoses of autoimmune blistering diseases with ELISA
Screening of autoimmune blistering diseases 11
Differential diagnosis of pemphigus 11
Differential diagnosis of BP 12
Differential diagnosis of epidermolysis bullosa acquisita (EBA) 12
Monitoring disease activities by ELISA
Monitoring disease activity in mucocutaneous PV with MESACUP Desmoglein ELISA kits 13
Monitoring disease activity in BP with MESACUP BP180 TEST 13
Monitoring disease activity in EBA with MESACUP Anti-Type VII collagen TEST 13
Acknowledgements / References
BOX
3
4
6
11
13
14
C O N T E N T S
TOPICS 9Desmoglein 1 is a target in bullous infectious diseases
10
Pemphigus
4 Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid - 5Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid -
Overview
Pemphigus is a group of autoimmune blistering diseases of the skin and mucous membranes which are characterizedhistologically by intraepidermal blisters due to acantholysis (i.e., disruption of the intercellular connections between keratinocytes of the epidermis) and immunopathologically by in vivo bound and circulating immunoglobulin G (IgG) antibodies directed against the cell surface of keratinocytes. Most common ages of disease onset is about 40 to 60 years. Nikolsky’s sign (i.e., blistering induced by lateral pressure to the normal-appearing skin) is also a characteristicfeature of pemphigus. The target antigens in pemphigus are Dsg1 and 3, 4, 5) members of the cadherin super family. Pemphiguscan be classified into pemphigus vulgaris (PV), pemphigus foliaceus (PF), paraneoplastic pemphigus (PNP), and others. The blisters in PV and PF occur in the deeper region of the epidermis (just above the basal layer) and the upper layer,respectively.
Clinical characterization
PV is the most common of pemphigus diseases. The
majority of patients have painful mucous membrane
erosions, especially in the oral cavity (Figure 1). While
mucous membranes are mainly affected in mucosal
dominant PV (MDPV), in mucocutaneous PV (MCPV),
blisters and erosions are not only present on the mucosal
area but also on the skin, predominantly the regions
prone to pressure and friction, such as scalp, axilla,
groin, upper part of back, and buttock. Pemphigus
vegetans, a rare form of PV, is characterized by vegetating
granulomatous lesions.
Pemphigus vulgaris (PV)
PF is characterized by scaly crusted erosions. These
lesions are scattered in seborrheic regions such as the
scalp, face, and upper trunk, while the mucous membranes
are never affected (Figure 2). Symptoms of patients with
PF are generally not as serious compared to those of PV.
Pemphigus erythematosus (Senear-Usher syndrome), the
localized form of PF, is associated with butterfly rash on
the face. Fogo selvagem (Brazilian pemphigus foliaceus)
is the endemic type of PF in the area of South America,
especially Brazil.
Pemphigus foliaceus (PF)
PNP is an autoimmune mucocutaneous disease associated
with underlying malignancy, particularly lymphoproliferative
neoplasms. Painful erosions and ulcerations occur in the
oral mucous membrane. In addition, many patients with
PNP have ocular mucosal lesions and pseudomembranous
conjunctivitis, resulting in ankyloblepharon in severe
cases. 6)
Paraneoplastic pemphigus (PNP)
Herpetiform pemphigus is characterized clinically by
erythematous urticarial plaques and vesicles that present
in a herpetiform arrangement, histologically eosinophilic
spongiosis with minimal or no acantholysis, and serologically
IgG autoantibodies against cell surfaces of keratinocytes.
Drug-induced pemphigus is induced by drugs such as
D-penicillamine or captopril. Neonatal pemphigus is a
disease that rarely occurs in infants born to mothers with
PV. IgA pemphigus is characterized by tissue-bound and
circulating IgA autoantibodies that target the desmosomal
proteins or unidentified cell surface antigens in the epidermis.
Other types of pemphigus
Oral lesion Histopathology
Acantholytic blisters in the epidermis are formed just above the basal layer.
Mucosal dominant PVIgG deposits on the cell surface of the epidermis, and stronger staining in the deeper layers than the upper layers.
Mucocutaneous PVIgG deposits on the cell surface throughout the epidermis.
Skin lesions
Direct immunofluorescence staining of the skins taken from patients with PV
Skin lesion Histopathology
IgG deposits on the cell surface of the epidermis,and stronger staining in the upper layers of the epidermis than the lower layers.
Acantholytic blisters in the epidermis are formed in the superficial epidermis.
Direct immunofluorescence staining ofthe skin taken from a patient with PF
Figure 1
Figure 2
Figure 3
Pemphigus vulgaris (PV, Mucosal dominant type)
Dsg1
Dsg3
Dsg3 function suppressed Dsg3 function suppressed
Dsg1 function suppressed Dsg1 function suppressed
Both Dsg1 & Dsg3 function suppressed Both Dsg1 & Dsg3 function suppressed
Dsg1
Dsg3
Pemphigus foliaceus (PF)
Dsg1
Dsg3
Dsg1
Dsg3
Pemphigus vulgaris (PV, Mucocutaneous type)
Dsg1
Dsg3
Dsg1
Dsg3
Anti-Dsg3Anti-Dsg1Dsg1 Dsg3
Skin lesion: None or only localized Mucosal lesion: Suprabasal epithelia
Skin lesion: Suprabasal epidermis Mucosal lesion: Suprabasal epithelia
Skin lesion: Superficial epidermis Mucosal lesion: None
Pemphigus (PV/PF) and anti-desmoglein 1 & 3 IgG autoantibodies
Dsg1 and Dsg3, the pemphigus target antigens, have
different intraepidermal expression patterns in the skin
and mucous membranes (Figure 3). In the skin, Dsg1 is
distributed throughout the epidermis, but more strongly
in the superficial layers, whereas Dsg3 is expressed
in the lower part of the epidermis (basal or parabasal
layers). In the mucous membranes, on the other hand,
Dsg1 and Dsg3 are expressed throughout the mucous
membrane, but the expression level of Dsg1 is much
lower than that of Dsg3. The clinical features of pemphigus
can be explained by “desmoglein compensation theory”,
i.e., these antigens can compensate their adhesive
functions when they are co-expressed in the same cells. 16, 17) In cases of PV, when only anti-Dsg3 antibodies are
present, the blister formations occur only in the deep
layers of mucous membranes that lack the compensation
by Dsg1 (mucosal-dominant type of PV). Patients who
have both anti-Dsg1 and anti-Dsg3 antibodies, the
blisters are formed in mucous membranes as well as
the skin (mucocutaneous type of PV). On the other hand,
in cases where antibodies are present only against Dsg1,
the blisters are formed only in the upper epidermis of
skin, where Dsg1 is present without compensation by
Dsg3 (PF). 9)
Pemphigoid
6 Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid - 7Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid -
Salt-split skin immunofluorescence
BP
IgG binds to the epidermal side of the split skin(indicated by arrow).
EBA
IgG binds to the dermal side of the split skin(indicated by arrow).
Overview
Pemphigoid is a group of diseases characterized histologically by subepidermal blisters and immunopathologically bylinear deposition of IgG and complement C3 at basement membrane zone (BMZ) in the skin from patients withcirculating IgG against the molecules within the dermal-epidermal junction (DEJ). The target antigens recognized byautoantibodies in patients with bullous pemphigoid (BP) are BP180 (a 180 kDa transmembrane protein), and BP230(a 230 kDa intracellular protein). The target antigens recognized by autoantibodies in other diseases of this groupinclude type VII collagen in epidermolysis bullosa acquisita (EBA); laminin 332 (laminin 5, epilligrin), one of the target antigens in mucous membrane pemphigoid (MMP); a 97 kDa protein (BP180 degradation product) in linear IgA bullousdermatoses (LAD); and laminin γ1 in anti-p200 pemphigoid. 10−12).
MMP had been called cicatricial pemphigoid due to
scar formation after blisters and erosions. However,
not all of the patients have scarring. MMP is a rare
autoimmune blistering disease, involving oral and ocular
mucous membranes. Linear depositions of IgG and/or
complement C3 along BMZ can be detected by direct
immunofluorescence assay. A major MMP target autoantigen
is BP180. Other target antigens include laminin 332 and
BP230. 14)
Mucous membrane pemphigoid (MMP)
EBA is a subepidermal autoimmune skin disease
associated with autoimmunity to type VII collagen (Figure
5), which is the major component of anchoring fibrils.
The classic presentation of EBA is noninflammatory
blistering on the extremities that heal with scarring and
milia formation.However, the clinical manifestation is
varied and inflammatory blisters and eruptions can also be
observed on any part of the body including the mucous
membrane. Histopathology shows subepidermal blisters
with different degrees of inflammation and neutrophil
infiltration. Direct immunofluorescence assay reveals
IgG deposition along BMZ. 15, 16)
Epidermolysis bullosa acquisita (EBA)
Dermatitis herpetiformis (DH) is characterized by chronic
eruptions typically on elbows, knees, and back with intense
pruritus. The granular deposits of IgA are detected in the
papillary dermis by direct immunofluorescence assay.
Circulating IgA autoantibodies against transglutaminase
have been identified in patients. However, the exact
mechanisms on the IgA deposition in the skin remain
unclear. In addition, it has been reported that the IgA
deposits may be reduced in the patients who go on a
long-term gluten-free diet. 17)
Dermatitis herpetiformis (Dühring disease)
LAD is a rare blistering disease with the onset over 40
years or under 10 years of age [chronic bullous diseases
of childhood (CBDC)]. The clinical manifestations of
LAD are itchy erythematous papules and blisters. Direct
immunofluorescence of perilesional skin from the patient
with LAD reveals IgA linear deposition along BMZ. A
target antigen is the 97 kDa protein, an extracellular
domain of BP180. 18)
Linear IgA dermatosis (LAD)
Anti-p200 pemphigoid is a blistering skin disease
occasionally seen in patients with psoriasis. Recently,
laminin γ1 was identified as the target antigen. 12)
Anti-p200 pemphigoid (Anti-laminin γ1 pemphigoid)
Skin lesion Histopathology
IgG deposits in BMZ.
Sub-epidermal blister formation.
Indirect immunofluorescence assay
Figure 4
Figure 5
Clinical characterization
The skin lesions of BP are characterized by tense blisters
with significant pruritus. Histopathological analysis
detects subepidermal blisters and superficial dermal
infiltrations of eosinophils, lymphocytes, and macrophages
(Figure 4). Mucous membrane erosions are occasionally
found in some patients with BP. BP usually occurs in
elderly individuals.
Herpes gestationis (HG, pemphigoid gestationis), a
subtype of BP, occurs during pregnancy and the immediate
postpartum period. 13) Histopathology of HG shows
subepidermal blisters with eosinophil infiltration.
Bullous pemphigoid (BP)
The localization of autoantibodies of EBA is distinct from the deposition in BP. To
differentiate EBA from BP, salt-split skin technique (i.e., skin incubated with 1 M NaCl to
fracture dermal-epidermal junctions) followed by direct immunofluorescence assay is
allowed to discriminate EBA from BP. The antibodies from the EBA patients are localized
at the dermal side of the separation.
Histopathology Direct immunofluorescence
Subepidermal blister formation. Linear deposition of IgG along BMZ.
Skin lesion
Pemphigoid
Staphylococcal scalded skin syndrome (SSSS) and bullous impetigo are blistering diseases caused by exotoxins (exfoliative
toxin, ET) produced by Staphylococcus aureus. SSSS is common in newborns, infants, and patients with renal failure or
immunodeficiency. It is considered that ET disseminated through the bloodstream causes erythema and blisters throughout
the body. Nikolsky’s sign is also detected. In bullous impetigo, however, ET produces the blisters locally at the infected area.
The mechanisms of blister formation in both diseases had remained unclear until recently, although classic studies showed that
ET could induce blisters in neonatal mice in the 1970’s.
SSSS and pemphigus foliaceus (PF) share many similar features; (1) only the skin is affected, but not the mucous membrane,
(2) the blister formation occurs in the upper epidermis, (3) no necrotic keratinocytes precede the blisters, and (4) injections
of ET into neonatal mice induce superficial blisters whose histology is identical to PF. In addition, various experiments
indicated that several ET subtypes (exfoliative toxin A, B, and D) induced the blister formation by a cleavage of Dsg1 at Gul381
through their serine protease activity, while they do not cleave Dsg3. This reflects the histological manifestation in SSSS, of
which the lesion is localized in the skin. It is clinically significant that the inactivation of Dsg1 causes superficial skin blisters in
two different skin diseases, PF and SSSS. 23, 24)
8 Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid - 9Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid -
Anti-BP180 autoantibodies in patients with BP are
generally considered to be pathogenic. In vitro studies
indicate that BP IgG activates the classical complement
pathway, thereby causing activation of inflammatory cells
with the degranulation and resulting dermal-epidermal
separation. 19) However, some reports suggested the
non-inflammatory mechanism of the blister formation;
anti-BP180 antibodies cause conformational changes
of BP180, to reduce functional BP180 molecules. 20) The
autoantibodies from most patients with BP recognize the
NC16a domain, which is a non-collageneous region of
BP180, located just outside the cell membrane.
In contrast, anti-BP230 antibodies may not directly
cause the blister formation because it is unlikely that the
antibodies can access to BP230 localized in the cytoplasm.
Nevertheless, anti-BP230 antibodies are a useful diagnostic
marker for BP with high specificity. Anti-BP230 antibodies
are detected only in some patients with BP. 21)
Autoantibodies against type VII collagen are associated
with dysfunction of anchoring fibrils in dermal-epidermal
junctions. Direct immunofluorescence staining shows
IgG deposition within the sub-lamina densa of the skin.
The localization of autoantibodies is distinct from the
deposition in BP. To differentiate EBA from BP, salt-split
skin technique (i.e., see page 7) followed by direct
immunofluorescence assay is allowed to discriminate
EBA from BP. The antibodies from the EBA patients are
localized at the dermal side of the separation.
Type VII collagen is composed of three identical alpha-
chains (290 kDa). Each chain consists of a 145 kDa
non-collagen (NC1) domain, a typical collageneous
domain, and a 34 kDa non-collagen (NC2) domain.
Epitopes recognized by autoantibodies from EBA
patients are mainly on NC1. NC2 is also considered to
contain minor epitopes. 22)
Bullous pemphigoid (BP) and anti-BP180 and anti-BP230 IgG autoantibodies
Epidermolysis bullosa acquisita (EBA) and anti-type VII collagen IgG autoantibodies
EBA
BP
Epidermal side
Dermal side
Epidermal side
Dermal side
ComplementNC16a
Blister
Anti-BP230
Anti-BP180
Anchoring fibril
BP180
BP230
Anchoring fibril
BP180
BP230
Anti-type VII collagen
Blister
Topic
Sites of the skin blister formation in BP and EBA
ET: Exfoliative toxin
Dsg1
ET
- Desmoglein 1 is a target in bullous infectious diseases -
Profile Kit Type VII collagenDSG 1
DSG 3
BP180
BP230
1 2 3 4 5 6 7 8 9 10 11 12ABCDEFGH
Calibrator 1 (0 U/mL)Calibrator 2 (100 U/mL)Dsg1Dsg3
A:B:C:D:
BP180BP230Type VII collagenAssay control (Human IgG)
E:F:G:H:
Detects 5 anti-skin antibodiesin a single assay Pemphigus Bullous pemphigoid EBA
epidermis side
dermis side
epidermis side
dermis side
Code No. Product Volume Storage Antigens / Description
RG-M7593-D
RG-M7612-D
RG-M7613-D
RG-7845R2
RG-7115R
48 wells
48 wells
48 wells
48 wells
8 wells x 12
2-8 °C
2-8 °C
2-8 °C
2-8 °C
2-8 °C
MESACUP Dsg1 & Dsg3 ELISA TEST SYSTEM
MESACUP BP180 TEST
MESACUP BP230 TEST
Anti-Type VII collagen ELISA Kit (For Research use only)
Anti-Skin Profile ELISA Kit (For Research use only)
Recombinant human Dsg1 and Dsg3
Recombinant human BP180 NC16a
Recombinant human BP230 (NT and CT)
Recombinant human type VII collagen NC1 and NC2
Recombinant human Dsg1, Dsg3, BP180, BP230 and type VII collagen
Code No. Product Volume Storage Antigens / Description
RG-7880EC-D
RG-7885EC-D
RG-7695EC-D
RG-7613EC-D
RG-7845E
RG-7115EC-D
48 wells
48 wells
48 wells
48 wells
48 wells
8 wells x 12
2-8 °C
2-8 °C
2-8 °C
2-8 °C
2-8 °C
2-8 °C
MESACUP-2 TEST Desmoglein 1
MESACUP-2 TEST Desmoglein 3
MESACUP BP180 TEST
MESACUP BP230 TEST
MESACUP Anti-Type VII collagen TEST
MESACUP Anti-Skin Profile TEST
Recombinant human Dsg1
Recombinant human Dsg3
Recombinant human BP180 NC16a
Recombinant human BP230 (NT and CT)
Recombinant human type VII collagen NC1 and NC2
Recombinant human Dsg1, Dsg3, BP180, BP230 and type VII collagen
For US customers
For EU customers
Value was determined by analysis with 30 PV, 30 PF, 60 BP, 30 EBA and 42 normal samples.
ELISA Index (U/mL)
Negative Positive
< 15 ≥ 15MESACUP Anti-Skin Profile TEST*
Concordance Disconcordance Concordance Rate (%)
Dsg1
Dsg3
BP180
BP230
Type VII collagen
189
191
191
189
189
3
1
1
3
3
98.4
99.5
99.5
98.4
98.4
Types of pemphigus Anti-Dsg3 antibody Anti-Dsg1 antibody
Mucosal-dominant PV
Mucocutaneous PV
PF
Positive
Positive
Negative
Negative
Positive
Positive
ELISA Index (U/mL)
Positive
≥ 20MESACUP-2 TEST Desmoglein 1†
MESACUP Dsg1 & Dsg3 ELISA TEST SYSTEM†† ≥ 20
MESACUP-2 TEST Desmoglein 3† ≥ 20
*U.S. Customers : for research use only (Not for use in diagnostic procedures)
† For EU Customers only†† For U.S. Customers only
10 Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid - 11Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid -
Differential diagnoses of autoimmune blistering diseases with ELISA
Differential diagnosis of pemphigus
Screening of autoimmune blistering diseases
Immunofluorescence assay may reveal differences in
staining patterns between PV and PF according to the
tissue distribution of Dsg1 and 3 (see page 4). However,
the immunofluorescence patterns of tissues are difficult
to clearly discriminate between the two diseases.
MESACUP Desmoglein ELISA kits are for measurements
of anti-Dsg1 and anti-Dsg3 antibodies in serum, using the
recombinant Dsg1 or Dsg3 as the solid-phase antigen.
These ELISA kits provide sensitive and specific assays
for the differential serological diagnosis between PV and
PF on the basis of their characteristic profiles of auto
antibodies. 25)
MESACUP Anti-Skin Profile ELISA TEST* is an ELISA
kit for the qualitative detection of IgG antibodies to Dsg1,
Dsg3, BP180, BP230 and type VII collagen in human
serum. These anti-skin autoantibodies can be detected
simultaneously in a single assay.
Interpretation of results with MESACUP Desmoglein ELISA kits
Disease classification of pemphigus by anti-Dsg antibody profiling
Presence of anti-Dsg1 and anti-Dsg3 antibodies in PV, PF, BP, and normal sera
Interpretation of results with MESACUP Anti-Skin Profile TEST*
Comparison of existing individual ELISA kits for autoimmuneblistering diseases and MESACUP Anti-Skin Profile TEST*
ELISA kits for the diagnosis of autoimmune blistering diseases
0
50
100
150
200
250Anti-Dsg1
PV(27/39)
PF(31/31)
BP(0/45)
Normal(0/180)
ELI
SA
Ind
ex
Anti-Dsg3
PV(39/39)
PF(0/31)
BP(1/45)
Normal(0/180)
20 20
ELISA Index (U/mL)
Negative Positive
< 9 ≥ 9
< 9
MESACUP BP180 TEST *1
MESACUP BP230 TEST *2 ≥ 9
Active stage Remission Total
MESACUP BP180 TEST
MESACUP BP230 TEST
MESACUP BP180 TEST +
MESACUP BP230 TEST
84% (54 / 64)
58% (37 / 64)
94% (60 / 64)
65% (113 / 175)
78% (136 / 175)
98% (172 / 175)
70% (167 / 239)
72% (173 / 239)
97% (232 / 239)
*1: Values were established by ROC analysis with 64 BP samples and control samples (42 PF, 69 PV and 336 normal samples).*2: Values were established by ROC analysis with 72 BP samples and 109 normal samples.
†Data courtesy of Kobayashi M, Amagai M, Kuroda-Kinoshita K, Hashimoto T, Shirakata Y, Hashimoto K, Nishikawa T. BP180 ELISA using bacterial recombinant NC16a protein as a diagnostic and monitoring tool for bullous pemphigoid. J. Dermatol. Sci. 30: 224-32, 2006, PubMed: 12443845
Values were determined by ROC analysis with 49 EBA, 20 PF, 20 BP and 266 normal samples.
ELISA Index (U/mL)
Negative Positive
< 6 ≥ 6MESACUP Anti-Type VII collagen TEST
Interpretation of results with MESACUP Anti-Type VII collagen TEST*
Presence of anti-type VII collagen antibodies in EBA, PV, BP, and normal sera ‡
*U.S. Customers : for research use only (Not for use in diagnostic procedures)‡Data for EU Customers only.*U.S. Customers : for research use only (Not for use in diagnostic procedures)
12 Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid - 13Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid -12 Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid - 13Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid -
Monitoring disease activities by ELISA
Clinical data using MESACUP Desmoglein kits suggest
that amounts of anti-Dsg1 and anti-Dsg3 antibodies
decrease during the improvement, correlating with the
improvement of cutaneous erosions. Amounts of
autoantibodies also correspond to the pemphigus disease
area index (PDAI).
In recent studies, the amount of anti-Dsg1 and anti-Dsg3
antibodies decreased significantly after rituximab and
intravenous immunoglobulin (IVIG) therapies. 29-31)
Monitoring disease activity in mucocutaneous PV with MESACUP Desmoglein ELISA kits
600
400
200
0
5040302010
0
Anti-
desm
ogle
in a
ntib
odie
s (U
/mL)
PDAI
0 14 37
Days after treatment
Anti-Dsg 3
Anti-Dsg 1
* PDAI: Pemphigus Disease Area Index
Days after treatment
Ant
i-typ
e VI
I col
lage
n an
tibod
ies
(U/m
L)
Days after treatment
6000
4000
2000
027 75 56 0
The amount of anti-type VII collagen antibodies decreased
with the improvement of cutaneous symptoms in a patient
with EBA after treatment. 28, 36, 37)
Monitoring disease activity in EBA with MESACUP Anti-Type VII collagen TEST*
Differential diagnosis of epidermolysis bullosa acquisita (EBA)
Differential diagnosis of BP
MESACUP Anti-Type VII collagen TEST is an ELISA kit
using the recombinant NC1 and NC2 domains of type VII
collagen for measurement of anti-type VII collagen
autoantibodies in human serum. Interestingly, 96%
(47/49) of EBA sera were positive with this kit, and none of
20 BP sera were positive. Thus, our ELISA kit provides a
sensitive and specific assay for the differential serological
diagnosis of EBA and BP. 28)‡
MESACUP BP180 TEST is an ELISA kit for the detection
of anti-BP180 antibodies in human serum, using the
recombinant BP180 NC16a protein as the immobilized
antigen. The sensitivity of the kit is 84% (54/64) in patients
with BP in the active stage. 26)
MESACUP BP230 TEST is an ELISA kit using both
the recombinant N-terminal and C-terminal domains
of BP230 for detection of anti-BP230 antibodies in
human serum. The sensitivity is 58% (37/64) in patients
diagnosed with BP in the active stage. Most significantly,
higher clinical sensitivity (97%) can be achieved by
combining the results of both BP180 and BP230 ELISA
kits. 27)
Interpretation of results with MESACUP BP180 and MESACUP BP230
Clinical sensitivity of anti-BP180 and anti-BP230 ELISA for BP sera†
Differential diagnoses of autoimmune blistering diseases with ELISA
ELI
SA
Ind
ex
Anti-BP230
BP(Active stage)
(37/64)
BP(Remission)(135/175)
PF/PV(1/94)
Normal(0/109)
0
50
100
150
200
250Anti-BP180
BP(Active stage)
(54/64)
BP(Remission)(113/175)
PV/PF(1/94)
Normal(5/336)
9 9
ELI
SA
Ind
ex
0
100
200
300
400
EBA(47/49)
PV(0/20)
BP(0/20)
Normal(1/266)
6
Presence of anti-BP180 and anti-BP230 antibodies in BP, PV/PF, and normal sera
Clinical manifestation of PV disease and anti-desmoglein antibody levels
Several clinical studies suggested that the data using
MESACAP BP180 TEST demonstrated that the
disappearance of blisters correlated with decrease in the
amount of anti-BP180 antibody. 27,33,34)
Additionally, in a previous report on one patient with
herpes gestationis (HG), the amount of anti-BP180
antibodies was consistent with the severity of the
erythema and blisters of mothers and neonates in the
peripartum period. 35) These findings strongly suggest
the clinical importance of periodic measurements of the
autoantibodies in patients with BP.
Monitoring disease activity in BP with MESACUP BP180 TEST
Anti-
BP18
0 an
tibod
ies
(U/m
L)
Days after treatment
1000
800
600
400
200
00 12 3528
Clinical manifestation of BP disease and anti-BP180 antibody levels
Clinical manifestation of EBA disease and anti-type VII collagen antibody levels
We are grateful to Drs. Masayuki Amagai and Jun Yamagami of Keio University School of Medicine for data and valuableadvice, and to Dr. Ken Ishii of Teikyo University Chiba Medical Center and Dr. Takashi Hashimoto of Kurume University School of Medicine for data.
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14 Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid - 15Autoimmune Blistering Diseases - Diagnostic Methodology for Pemphigus and Pemphigoid -
Acknowledgements
References
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