Hemolytic Biomarkers Predict Adhesiveness of Sickle Blood Cells in a Clinical Adhesion Bioassay

Sickle cell disease (SCD) is characterized by frequent and unpredictable vaso-occlusive episodes (VOEs) that produce severe pain, organ damage, and early death. Lack of reliable biomarkersto objectively define VOEs, hindersthe development of clinically useful interventions to improve the care for th...

Full description

Saved in:
Bibliographic Details
Published inBlood Vol. 136; no. Supplement 1; p. 31
Main Authors White, Jennell, Gao, Xiufeng, Tarasev, Michael, Liu, Ke, Callaghan, Michael U., Hines, Patrick C.
Format Journal Article
LanguageEnglish
Published Elsevier Inc 05.11.2020
Online AccessGet full text
ISSN0006-4971
1528-0020
DOI10.1182/blood-2020-143402

Cover

Abstract Sickle cell disease (SCD) is characterized by frequent and unpredictable vaso-occlusive episodes (VOEs) that produce severe pain, organ damage, and early death. Lack of reliable biomarkersto objectively define VOEs, hindersthe development of clinically useful interventions to improve the care for these patients.VOEs result from a complex interplay of adhesive eventsmediated by cell surface adhesion molecules elevated in the SCD microenvironment. We developed a clinical adhesion assay that incorporates the adhesive properties of mature erythrocytes, reticulocytes, and leukocytes to measure adhesion from blood samples obtained from SCD subjects. Blood is acquired by venipuncture in sodium citrate tubes and can be stored for up 48hrs at 4°C.Flow conditions (37°C, 1.0 dyne/cm2, 1.67Hz) mimic blood flow in the post-capillary venules where these adhesive interactions are likely to occur. Adherent cells are quantified within a standard viewing area (cells/mm2) to generate an adhesion index(AI).Adhesion was evaluated in SCD subjects in a 6-month, longitudinal, observational study. Hematologic lab values were obtained at each blood draw. An electronic patient reported outcome (ePRO) tool defined steady state and VOE status. We have shown that AIs are elevated in SCD subjects with severe disease phenotypes and during VOEs and decreased in SCD subjects receiving SCD-modifying therapies. The objective of this study was to identify hematologic lab values that contribute to cellular adhesion in our clinical adhesion bioassay. A multi-variantmixed-effects regression model was used to allow for the estimation of different item factor loadings (regression coefficients) for the multiple outcomes. Coefficient of determination for each variable or model was calculated using MuMin package in Rstatistical software.Here, we report that a lower hematocrit (Hct) and higher reticulocyte percent (retic %) predicts (24%; p=0.009) cellular adhesiveness in blood samples collected from SCD subjects at steady state. However, adhesive predictors vary during VOE (Hct or hemoglobin F-HbF). Our findings suggest that cellular adhesiveness in SCD, as assessed by our clinical adhesion assay, may be a surrogate for clinical state and/or identifying impending VOEs. Further studies are needed to validate the utility of the adhesion bioassay in assessing the clinical utility of adhesion as a biomarker in clinical practice. White:Functional Fluidics:Current equity holder in private company.Gao:Functional Fluidics:Current equity holder in private company.Tarasev:Functional Fluidics:Current equity holder in private company.Liu:Functional Fluidics:Current equity holder in private company.Callaghan:Octapharma:Honoraria, Membership on an entity's Board of Directors or advisory committees;Spark:Honoraria, Membership on an entity's Board of Directors or advisory committees;Biomarin:Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Site Investigator/sub-I Clinical Trial, Speakers Bureau;Bioverativ:Membership on an entity's Board of Directors or advisory committees;Shire:Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau;Grifols:Honoraria, Membership on an entity's Board of Directors or advisory committees;Bayer:Honoraria, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau;Roche/Genentech:Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Site Investigator/sub-I Clinical Trial, Speakers Bureau;Sancillio:Other;Alnylum:Current equity holder in publicly-traded company;NovoNordisk:Other, Speakers Bureau;Global Blood Therapeutics:Honoraria, Membership on an entity's Board of Directors or advisory committees, Other, Speakers Bureau;Pfizer:Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Site Investigator/sub-I Clinical Trial, Research Funding;Hema Biologics:Honoraria, Membership on an entity's Board of Directors or advisory committees.Hines:Functional Fluidics:Current equity holder in private company.
AbstractList Sickle cell disease (SCD) is characterized by frequent and unpredictable vaso-occlusive episodes (VOEs) that produce severe pain, organ damage, and early death. Lack of reliable biomarkersto objectively define VOEs, hindersthe development of clinically useful interventions to improve the care for these patients.VOEs result from a complex interplay of adhesive eventsmediated by cell surface adhesion molecules elevated in the SCD microenvironment. We developed a clinical adhesion assay that incorporates the adhesive properties of mature erythrocytes, reticulocytes, and leukocytes to measure adhesion from blood samples obtained from SCD subjects. Blood is acquired by venipuncture in sodium citrate tubes and can be stored for up 48hrs at 4°C.Flow conditions (37°C, 1.0 dyne/cm2, 1.67Hz) mimic blood flow in the post-capillary venules where these adhesive interactions are likely to occur. Adherent cells are quantified within a standard viewing area (cells/mm2) to generate an adhesion index(AI).Adhesion was evaluated in SCD subjects in a 6-month, longitudinal, observational study. Hematologic lab values were obtained at each blood draw. An electronic patient reported outcome (ePRO) tool defined steady state and VOE status. We have shown that AIs are elevated in SCD subjects with severe disease phenotypes and during VOEs and decreased in SCD subjects receiving SCD-modifying therapies. The objective of this study was to identify hematologic lab values that contribute to cellular adhesion in our clinical adhesion bioassay. A multi-variantmixed-effects regression model was used to allow for the estimation of different item factor loadings (regression coefficients) for the multiple outcomes. Coefficient of determination for each variable or model was calculated using MuMin package in Rstatistical software.Here, we report that a lower hematocrit (Hct) and higher reticulocyte percent (retic %) predicts (24%; p=0.009) cellular adhesiveness in blood samples collected from SCD subjects at steady state. However, adhesive predictors vary during VOE (Hct or hemoglobin F-HbF). Our findings suggest that cellular adhesiveness in SCD, as assessed by our clinical adhesion assay, may be a surrogate for clinical state and/or identifying impending VOEs. Further studies are needed to validate the utility of the adhesion bioassay in assessing the clinical utility of adhesion as a biomarker in clinical practice. White:Functional Fluidics:Current equity holder in private company.Gao:Functional Fluidics:Current equity holder in private company.Tarasev:Functional Fluidics:Current equity holder in private company.Liu:Functional Fluidics:Current equity holder in private company.Callaghan:Octapharma:Honoraria, Membership on an entity's Board of Directors or advisory committees;Spark:Honoraria, Membership on an entity's Board of Directors or advisory committees;Biomarin:Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Site Investigator/sub-I Clinical Trial, Speakers Bureau;Bioverativ:Membership on an entity's Board of Directors or advisory committees;Shire:Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau;Grifols:Honoraria, Membership on an entity's Board of Directors or advisory committees;Bayer:Honoraria, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau;Roche/Genentech:Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Site Investigator/sub-I Clinical Trial, Speakers Bureau;Sancillio:Other;Alnylum:Current equity holder in publicly-traded company;NovoNordisk:Other, Speakers Bureau;Global Blood Therapeutics:Honoraria, Membership on an entity's Board of Directors or advisory committees, Other, Speakers Bureau;Pfizer:Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Site Investigator/sub-I Clinical Trial, Research Funding;Hema Biologics:Honoraria, Membership on an entity's Board of Directors or advisory committees.Hines:Functional Fluidics:Current equity holder in private company.
Sickle cell disease (SCD) is characterized by frequent and unpredictable vaso-occlusive episodes (VOEs) that produce severe pain, organ damage, and early death. Lack of reliable biomarkersto objectively define VOEs, hindersthe development of clinically useful interventions to improve the care for these patients.VOEs result from a complex interplay of adhesive eventsmediated by cell surface adhesion molecules elevated in the SCD microenvironment. We developed a clinical adhesion assay that incorporates the adhesive properties of mature erythrocytes, reticulocytes, and leukocytes to measure adhesion from blood samples obtained from SCD subjects. Blood is acquired by venipuncture in sodium citrate tubes and can be stored for up 48hrs at 4°C.Flow conditions (37°C, 1.0 dyne/cm2, 1.67Hz) mimic blood flow in the post-capillary venules where these adhesive interactions are likely to occur. Adherent cells are quantified within a standard viewing area (cells/mm2) to generate an adhesion index(AI).Adhesion was evaluated in SCD subjects in a 6-month, longitudinal, observational study. Hematologic lab values were obtained at each blood draw. An electronic patient reported outcome (ePRO) tool defined steady state and VOE status. We have shown that AIs are elevated in SCD subjects with severe disease phenotypes and during VOEs and decreased in SCD subjects receiving SCD-modifying therapies. The objective of this study was to identify hematologic lab values that contribute to cellular adhesion in our clinical adhesion bioassay. A multi-variantmixed-effects regression model was used to allow for the estimation of different item factor loadings (regression coefficients) for the multiple outcomes. Coefficient of determination for each variable or model was calculated using MuMin package in Rstatistical software.Here, we report that a lower hematocrit (Hct) and higher reticulocyte percent (retic %) predicts (24%; p=0.009) cellular adhesiveness in blood samples collected from SCD subjects at steady state. However, adhesive predictors vary during VOE (Hct or hemoglobin F-HbF). Our findings suggest that cellular adhesiveness in SCD, as assessed by our clinical adhesion assay, may be a surrogate for clinical state and/or identifying impending VOEs. Further studies are needed to validate the utility of the adhesion bioassay in assessing the clinical utility of adhesion as a biomarker in clinical practice.
Author Gao, Xiufeng
Liu, Ke
Hines, Patrick C.
White, Jennell
Tarasev, Michael
Callaghan, Michael U.
Author_xml – sequence: 1
  givenname: Jennell
  surname: White
  fullname: White, Jennell
  organization: Department of Pediatrics Pharmacology, Wayne State University School of Medicine, Detroit, MI
– sequence: 2
  givenname: Xiufeng
  surname: Gao
  fullname: Gao, Xiufeng
  organization: Functional Fluidics, Detroit, MI
– sequence: 3
  givenname: Michael
  surname: Tarasev
  fullname: Tarasev, Michael
  organization: Functional Fluidics LLC., Detroit, MI
– sequence: 4
  givenname: Ke
  surname: Liu
  fullname: Liu, Ke
  organization: Functional Fluidics, Detroit, MI
– sequence: 5
  givenname: Michael U.
  surname: Callaghan
  fullname: Callaghan, Michael U.
  organization: Central Michigan University, Children's Hospital of Michigan, Detroit, MI
– sequence: 6
  givenname: Patrick C.
  surname: Hines
  fullname: Hines, Patrick C.
  organization: Functional Fluidics, Detroit, MI
BookMark eNp9kMFKAzEQhoNUsK0-gLe8wGomzW43eGoXtUJBwd5DNpnF2HQjyVLo25u1PXuaYZj_n_m_GZn0oUdC7oE9ANT8sfUh2IIzzgoQC8H4FZlCyeuC5dGETBljVSHkEm7ILKVvxvIWL6dEbfAQ_Glwhq5dOOi4x5joR0TrzEBX9guTO2KPKdHQ0U9n9h7pejxGG_Q-UddTTRvveme0vwhCP5rplPTpllx32ie8u9Q52b0875pNsX1_fWtW28JIwYuSaVHqKvegBbYaWmBW1gCaG2b1ooUK67qVdSmNLZeV1MJoWbVL04HlVbeYEzjbmhhSitipn-hympMCpkZA6g-QGgGpM6CseTprMP91dBhVMg57k6NHNIOywf2j_gW5DnB2
ContentType Journal Article
Copyright 2020 American Society of Hematology
Copyright_xml – notice: 2020 American Society of Hematology
DBID AAYXX
CITATION
DOI 10.1182/blood-2020-143402
DatabaseName CrossRef
DatabaseTitle CrossRef
DatabaseTitleList
CrossRef
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Chemistry
Biology
Anatomy & Physiology
EISSN 1528-0020
EndPage 31
ExternalDocumentID 10_1182_blood_2020_143402
S0006497118726475
GroupedDBID ---
-~X
.55
1CY
23N
2WC
34G
39C
4.4
53G
5GY
5RE
5VS
6J9
AAEDW
AAXUO
ABOCM
ABVKL
ACGFO
ADBBV
AENEX
AFOSN
AHPSJ
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
BAWUL
BTFSW
CS3
DIK
DU5
E3Z
EBS
EJD
EX3
F5P
FDB
FRP
GS5
GX1
IH2
K-O
KQ8
L7B
LSO
MJL
N9A
OK1
P2P
R.V
RHF
RHI
ROL
SJN
THE
TR2
TWZ
W2D
W8F
WH7
WOQ
WOW
X7M
YHG
YKV
ZA5
0R~
AALRI
AAYXX
ACVFH
ADCNI
ADVLN
AEUPX
AFPUW
AIGII
AITUG
AKBMS
AKRWK
AKYEP
CITATION
EFKBS
H13
ID FETCH-LOGICAL-c942-50a45a6c941a4eba1b10d9811a2c0da3b16e88b9859cd5769a4ca96b7cf1d26f3
ISSN 0006-4971
IngestDate Wed Oct 01 00:31:41 EDT 2025
Fri Feb 23 02:43:32 EST 2024
IsPeerReviewed true
IsScholarly true
Issue Supplement 1
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c942-50a45a6c941a4eba1b10d9811a2c0da3b16e88b9859cd5769a4ca96b7cf1d26f3
PageCount 1
ParticipantIDs crossref_primary_10_1182_blood_2020_143402
elsevier_sciencedirect_doi_10_1182_blood_2020_143402
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2020-11-05
2020-11-5
PublicationDateYYYYMMDD 2020-11-05
PublicationDate_xml – month: 11
  year: 2020
  text: 2020-11-05
  day: 05
PublicationDecade 2020
PublicationTitle Blood
PublicationYear 2020
Publisher Elsevier Inc
Publisher_xml – name: Elsevier Inc
SSID ssj0014325
Score 2.3454807
Snippet Sickle cell disease (SCD) is characterized by frequent and unpredictable vaso-occlusive episodes (VOEs) that produce severe pain, organ damage, and early...
SourceID crossref
elsevier
SourceType Index Database
Publisher
StartPage 31
Title Hemolytic Biomarkers Predict Adhesiveness of Sickle Blood Cells in a Clinical Adhesion Bioassay
URI https://dx.doi.org/10.1182/blood-2020-143402
Volume 136
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVAFT
  databaseName: Open Access Digital Library
  customDbUrl:
  eissn: 1528-0020
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0014325
  issn: 0006-4971
  databaseCode: KQ8
  dateStart: 19460101
  isFulltext: true
  titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html
  providerName: Colorado Alliance of Research Libraries
– providerCode: PRVBFR
  databaseName: Free Medical Journals
  customDbUrl:
  eissn: 1528-0020
  dateEnd: 20241004
  omitProxy: true
  ssIdentifier: ssj0014325
  issn: 0006-4971
  databaseCode: DIK
  dateStart: 19460101
  isFulltext: true
  titleUrlDefault: http://www.freemedicaljournals.com
  providerName: Flying Publisher
– providerCode: PRVFQY
  databaseName: GFMER Free Medical Journals
  customDbUrl:
  eissn: 1528-0020
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0014325
  issn: 0006-4971
  databaseCode: GX1
  dateStart: 0
  isFulltext: true
  titleUrlDefault: http://www.gfmer.ch/Medical_journals/Free_medical.php
  providerName: Geneva Foundation for Medical Education and Research
– providerCode: PRVLSH
  databaseName: Elsevier Journals
  customDbUrl:
  mediaType: online
  eissn: 1528-0020
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0014325
  issn: 0006-4971
  databaseCode: AKRWK
  dateStart: 19460101
  isFulltext: true
  providerName: Library Specific Holdings
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lj9MwELbKIh4XBF0Qy0s-IA5UWWLHSZzjtjwKaDkVqbfIThwRKU1Qt0Vajvxyxq803YfEconcSJmmnq8zY8_nGYRe81CCH5VloCrBAyZhlFUkCUqlIkbLSArTkuX0WzL_zr4s4-Vo9GfAWtpu5HHx-8pzJf-jVbgHetWnZG-g2V4o3IAx6BeuoGG4_pOO52rVNee65Oq07laaaLM-06SKsi50Wdwf6szbMn00pdZZ3MlUM9UnM9U0hgkrJjN_NtI-AGgAYRBSi_2Eb-O6yh8Pu-ppboxqepLGJ2E2Xpf1tlLOI5pNgTW4yl8XSfqaBVRv7dmg4d4DLDT1fmq8Z08T3aPOokM5E6prXoc03LOxtsqJA5NpWGp2PydkYDydO1CDD5cNPNcFYy2p374Ri1hId97MZ_AvOLmeemgWPZzmRkSuReRWxC10m6YJ0wv495-_9pkoFlHbBcP9UpcZBxHvLr3F1bHNIF5ZPEQP3EIDn1jUPEIj1Y7R4UkrNt3qHL_BhvprcipjdGfqR_dmvgHgGN09dbyLQ5T3SMM7pGGHNDxEGu4qbJGGDWSwQRquWyywRxr2SMMeaY_R4uOHxWweuNYcQZExGsShYLFIYEwEU1IQScIy44QIWoSliCRJFOcy43FWlLCizQQrRJbItKhISZMqeoIO2q5VTxHOVKJ7k2SFSDmTRIqkSnlFBRMpKWBOj9BbP6f5T1uAJb9Wh0eI-VnPXQRpI8Mc8HP9Y89u8h3P0f3dX-EFOtist-olBKYb-cog5y8HNoy0
linkProvider Flying Publisher
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Hemolytic+Biomarkers+Predict+Adhesiveness+of+Sickle+Blood+Cells+in+a+Clinical+Adhesion+Bioassay&rft.jtitle=Blood&rft.au=White%2C+Jennell&rft.au=Gao%2C+Xiufeng&rft.au=Tarasev%2C+Michael&rft.au=Liu%2C+Ke&rft.date=2020-11-05&rft.issn=0006-4971&rft.eissn=1528-0020&rft.volume=136&rft.issue=Supplement+1&rft.spage=31&rft.epage=31&rft_id=info:doi/10.1182%2Fblood-2020-143402&rft.externalDBID=n%2Fa&rft.externalDocID=10_1182_blood_2020_143402
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0006-4971&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0006-4971&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0006-4971&client=summon