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Variable Short NameVariable Long NameVariable Description and Usage NotesOrder of the VariableControlled TerminologyAdditional Notes
--SCMBCLSecreted Molecule by Cells

Usage: This is a domain specific variable, and qualifies the ISTEST variable.

Description: The textual description of the entity secreted by the cells represented in the ISTEST. The combination of ISTEST and ISSCMBCL should describe "the thing, the entity or the analyte" one is measuring, without the need of additional variables.

It is placed right after BDAGNTNo. Free-text description.

--BDAGNT


Binding Agent


Usage: This is a domain specific variable, and qualifies the ISTEST variable.

Description: The textual description of the agent that's binding to the entity in the ISTEST variable. The ISBDAGNT variable is used to indicate that there is a binding relationship between the entities in the ISTEST and ISBDAGNT variables, regardless of direction.

ISBDAGNT is not a method qualifier. It should only be used when the actual interest of the measurement is the binding interaction between the two entities in ISTEST and ISBDAGNT. In other words, the combination of ISTEST and ISBDAGNT should describe "the thing, the entity or the analyte" one is measuring, without the need of additional variables.

The binding agent may be, but not limited to, a test article, a portion of the test article, a related compound, an endogenous molecule, an allergen or an infectious agent.

It is placed right after ISTEST. (this is used more than SCMBCL)

Yes. Two codelists.

-Microorgansim (MICROORG)

-Binding Agent for Immunogenicity Assessments (ISBDAGT).


--TSTOPO

Test Operational Objective

Usage: This is a domain-specific variable for LB and IS that qualifies the --TEST variable. This is a permissible variable.

Description: The textual description of the high-level purpose of the test at the operational level.

It is placed right after ISTSTDTL.

*When getting this ready for internal review, make sure to add TSTDTL into the IS specification table.

Yes. One codelist.

Codelist Rules: this is a non-extensible codelist and the MB SDS/CT team reserves the right to review future term request to this codelist and decide whether addition of new terms are appropriate.

Controlled Terminology:

-SCREEN: A test whose operational purpose is to determine the presence or absence of a substance or organism.

-CONFIRM: A test whose operational purpose is to verify the presence or absence of a substance or organism.

-QUANTIFY: A test whose operational purpose is to determine the amount or concentration of a substance or organism.

  1. use-case examples for "Quantify" are: measurements of any types of antibody titer (titration), viral load, bacterial colony count, drug toxicity concentration, etc.
  2. drug toxicity concentration: appears often in LOINC mapping. Also see example: https://wiki.cdisc.org/x/Qx3JB


Notes for Variable Name/Description:

  1. Analytical purpose vs operational purpose of a test - there is a difference between the two, analytical purpose is about the analyte itself - what specific analyte are you measuring, which is why in lab we tend to have the analyte name as the LBTEST - LBTEST tells the analyte of interest. The operational purpose/objective of an analyte test is to screen, confirm then quantify the analyte - this represents a different level of purpose, and operational purpose can be applied to any analyte hence it is not analyte-specific.

    Take ADA as an example, ISTEST = Binding Antidrug Antibody, this test tells you that you are looking for ADAs, not, for example, C-reactive proteins. The Screen, Confirm and Quantify then tell you the operational reason, the whys behind each performed ADA test.

  2. REAS (Currently NSV) : it is been proposed to name this variable as REAS/Reasons Done, or at least re-use this variable. This idea is rejected because we want to control this variable with very specific values and use-cases and REAS has been used in many TAUGs with all kinds of values. We do not want to confuse people who are already using REAS.


Controlled Terminology Notes:

Is "Detection" a valid value for this codelist? We had said before that one should use "detection" when one does not know whether the test is for screening or confirmatory, however is this a synonym to screen? look at the definition for screening, how is it different from detection? Confirm is to verify the previously detected substance is present.

  • Sponsor feedback is that "detected" is normally reported as a result hence this value does not belong in this codelist, because both screen and confirm are to detect the analyte, they are test qualifiers.

How about "quantify to confirm", what does that mean, is this also a valid value?

  • Ine mentioned that sometimes you would perform a quantificaiton test to confirm the existence of a substance. In this instance you get a quantitative result which confirms the existence of the substance, from which you normally only report "Positive or Negative" as confirmation. However the PURPOSE of the test is still to confirm the substance, so even though in the process you are using a quantitative method, the high-level purpose is to confirm. In this instance, the correct TSTOPO value to use is still "CONFIRM". Quantitative is an attribute of the method.

Example 1: Tiered Testing of ADA

This example shows the tiered testing of antidrug antibody (ADA). Typical tiered testing scheme for ADA evaluation includes the following steps: screening, confirmatory, and "characterization". In the first tier, all evaluable samples are run in the screen assay. Samples that score positive in the screen assay are then analyzed in a confirmatory assay (tier 2). Samples that are positive for ADA in the screen and confirmatory tiers are reported as positive, while samples that are negative in either tier are reported as negative. Further tiered testing of positive samples frequently includes analysis of antibody titer and neutralizing activity. The variable "TSTOPO" has the following controlled values: SCREEN, CONFIRM and QUANTIFY to describe the operational objective or the reason behind each testing step, and also to provide uniqueness to each row of record. ISGRPID is used in this example to show that the records are related to each other, and in this case, tests are done in a tiered, sequential manner.

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Row 1:Shows the screening of the presence of ADA to DRUG AZ-007.
Row 2:Shows the confirmation of the previously detected ADA to DRUG AZ-007.
Row 3:Shows the quantification of the said ADA from the screen and confirmatory steps.



Dataset2


RowSTUDYIDDOMAINUSUBJIDISSEQISREFID ISGRPIDISTESTCDISTEST

ISBDAGNT

ISTSTOPOISCATISSCATISORRESISORRESUISSTRESCISSTRESN ISSTRESUISSPECISMETHODVISITNUMVISITISDTC
 1 ABCIS  ABC-002 1 V5551

ADA_BAB

Binding Antidrug Antibody

DRUG AZ-007

SCREEN

ANTIDRUG ANTIBODIES

 
HUMORAL IMMUNITYPOSITIVE 
POSITIVE 

SERUM ELECTROCHEMILUMINESCENCE IMMUNOASSAY 1VISIT 12017-07-27
 2 ABC IS ABC-002 2 V5551ADA_BABBinding Antidrug Antibody

DRUG AZ-007

CONFIRM

ANTIDRUG ANTIBODIESHUMORAL IMMUNITYPOSITIVE 
POSITIVE 

SERUMELECTROCHEMILUMINESCENCE IMMUNOASSAY 1VISIT 12017-07-27
 3 ABCIS  ABC-002 3 V5551

ADA_BAB

Binding Antidrug Antibody

DRUG AZ-007

QUANTIFY

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITY50titer5050titerSERUM ELECTROCHEMILUMINESCENCE IMMUNOASSAY 1VISIT 12017-07-27



Nsvmeta
DomainIS


VariableLabelTypeRoleOrigin
ISTSTOPO Test Operational ObjectivetextNon-Standard Record QualifierCRF



Example 2: Consolidated Reporting of ADA

The example below shows how to represent the various types of antidrug antibody tests (ADA). Of note, while most ADAs do not inhibit the pharmacodynamic activity of the drug, neutralizing antidrug antibodies (NAbs) can inhibit drug activity soon after the drug is administered. However, most ADAs, or rather, the non-NAbs can lower the drug's systemic exposure just as well by increasing the rate of drug clearance, resulting in a clinically similar outcome to that of Nabs – reduced clinical efficacy.

...

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Rows 1-2:Show the confirmation and quantification of binding ADA to coagulation factor VIII analogue drug. A binding antidrug antibody is an antibody that binds to a drug.
Rows 3-4:Show the confirmation and quantification of the neutralizing binding ADA to coagulation factor VIII analogue drug. A neutralizing binding antidrug antibody is a type of ADA that binds to the functional portion of a drug leading to diminished or negated pharmacological activity. The neutralizing ADAs are a subset of the total ADAs.
Rows 5-6:Show the confirmation and quantification of the cross-reactive binding ADA to the endogenous coagulation factor VIII. A cross-reactive binding antidrug antibody is a type of ADA that binds to endogenous molecules, they are also a subset of the total ADAs.
Rows 7-8:Show the confirmation and quantification of the neutralizing cross-reactive binding ADA to the endogenous coagulation factor VIII. A neutralizing cross-reactive binding antidrug antibody is a type of ADA that binds to endogenous molecules and diminishes or negates their function; in some cases, they may also bind and negate the function of the study drug. They are a subset of the total ADAs.



Dataset2


RowSTUDYIDDOMAINUSUBJIDISSEQISREFIDISGRPIDISTESTCDISTEST

ISBDAGNT

ISCATISSCAT ISORRESISORRESUISSTRESCISSTRESN ISSTRESUISSPECISMETHODVISITNUMVISITISDTC
ISTSTOPO
 1 ABCIS  ABC-001 1A428391

ADA_BAB

Binding Antidrug Antibody

COAGULATION FACTOR VIII ANALOGUE DRUG

ANTIDRUG ANTIBODIES

 
HUMORAL IMMUNITY POSITIVE 
POSITIVE 

SERUM 

ELECTROCHEMILUMINESCENCE IMMUNOASSAY

 1VISIT 12017-07-27
CONFIRM
 2 ABCIS  ABC-001 2A428391

ADA_BAB

Binding Antidrug Antibody

COAGULATION FACTOR VIII ANALOGUE DRUG

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITY30 titer30 30 titerSERUM ELECTROCHEMILUMINESCENCE IMMUNOASSAY 1VISIT 12017-07-27
QUANTIFY

 3

 ABCIS  ABC-001 3 A428392

ADA_NAB

Neutralizing Binding Antidrug Antibody

COAGULATION FACTOR VIII ANALOGUE DRUG

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITYPOSITIVE 
POSITIVE 

SERUM 

HEMAGGLUTINATION INHIBITION ASSAY

 1VISIT 12017-07-27
CONFIRM
 4 ABCIS  ABC-001 4 A428392

ADA_NAB


Neutralizing Binding Antidrug Antibody

COAGULATION FACTOR VIII ANALOGUE DRUG

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITY60 titer60 60 titerSERUM 

HEMAGGLUTINATION INHIBITION ASSAY

 1VISIT 12017-07-27
QUANTIFY
 5 ABCIS  ABC-001 5 A428393

ADA_X

Cross-Reactive Binding Antidrug Antibody

ENDOGENOUS COAGULATION FACTOR VIII

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITYPOSITIVE 
POSITIVE 

SERUM  ELECTROCHEMILUMINESCENCE IMMUNOASSAY 1VISIT 12017-07-27
CONFIRM
 6 ABCIS  ABC-001 6 A428393

ADA_X

Cross-Reactive Binding Antidrug Antibody

ENDOGENOUS COAGULATION FACTOR VIII

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITY360 titer360 360 titerSERUM  ELECTROCHEMILUMINESCENCE IMMUNOASSAY 1VISIT 12017-07-27
QUANTIFY
 7 ABCIS  ABC-001 7 A428394

ADA_NX

Neutralizing Cross-Reactive Binding Antidrug Antibody

ENDOGENOUS COAGULATION FACTOR VIII

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITYPOSITIVE 
POSITIVE 

SERUM 

HEMAGGLUTINATION INHIBITION ASSAY

 1VISIT 12017-07-27
CONFIRM
 8 ABCIS  ABC-001 8 A428394

ADA_NX

Neutralizing Cross-Reactive Binding Antidrug Antibody

ENDOGENOUS COAGULATION FACTOR VIII

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITY360 titer360 360 titerSERUM 

HEMAGGLUTINATION INHIBITION ASSAY

 1VISIT 12017-07-27
QUANTIFY



Nsvmeta
DomainIS


VariableLabelTypeRoleOrigin
ISTSTOPO Test Operational ObjectivetextNon-Standard Record QualifierCRF



Example 3 - ADA Reaction Against Drug Components - Breakdown Product

This example shows the production of antidrug antibody in response to both the prodrug and its active metabolite. A prodrug is a compound that, after administration, is metabolized into a pharmacologically active drug. Please note in this example, even though only confirmatory records are reported and shown, it is assumed that the screening step has also been performed.

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Rows 1-2:Show the confirmation and quantification of the ADA against the prodrug A.
Rows 3-4:Show the confirmation and quantification of the ADA against the active metabolite of the prodrug A.



Dataset2


RowSTUDYIDDOMAINUSUBJIDISSEQISREFID ISGRPIDISTESTCDISTESTISBDAGNTISCATISSCATISORRESISORRESUISSTRESCISSTRESN ISSTRESUISSPECISMETHODVISITNUMVISITISDTC
ISTSTOPO
 1 ABCIS  ABC-004 1 J1231

ADA_BAB

Binding Antidrug Antibody

PRODRUG A

ANTIDRUG ANTIBODIES

 
HUMORAL IMMUNITYPOSITIVE 
POSITIVE 

SERUM ELECTROCHEMILUMINESCENCE IMMUNOASSAY 1VISIT 12017-07-27

CONFIRM

 2 ABCIS  ABC-004 2 J1231

ADA_BAB

Binding Antidrug Antibody

PRODRUG A

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITY30 titer30 30 titerSERUM ELECTROCHEMILUMINESCENCE IMMUNOASSAY 1VISIT 12017-07-27
QUANTIFY

 3

 ABCIS  ABC-004 3 J1232

ADA_BAB

Binding Antidrug Antibody

PRODRUG A ACTIVE METABOLITE

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITYPOSITIVE 
POSITIVE 

SERUM ELECTROCHEMILUMINESCENCE IMMUNOASSAY 1VISIT 12017-07-27

CONFIRM

 4 ABCIS  ABC-004 4 J1232

ADA_BAB


Binding Antidrug Antibody

PRODRUG A ACTIVE METABOLITE

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITY60 titer60 60 titerSERUM ELECTROCHEMILUMINESCENCE IMMUNOASSAY 1VISIT 12017-07-27
QUANTIFY



Nsvmeta
DomainIS


VariableLabelTypeRoleOrigin
ISTSTOPOTest Operational ObjectivetextNon-Standard Record QualifierCRF



Example 4 - ADA Reaction Against Drug Components: Multiple Epitopes per Molecule

The example below shows the production of antidrug antibody in response to both the study biologic drug and also to different immunogenic epitopes of the biologic drug. This also captures an example for when the tier stops at screening (interferon beta1a assay) and goes straight into NAB from there. While unusual, it reflects the flexibility of these fields to incorporate multiple options.

...

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Row 1:Shows the presence of ADA against the active motabolite (active interferon beta 1a portion) of peginterferon beta-1a.
Rows 2-3:Show the screening and confirmation of ADA against the PEG epitope portion of peginterferon beta-1a.
Rows 4-5:Show the presence and quantification of neutralizing ADA against the whole molecule peginterferon beta-1a.
Row 6:Shows the absence of ADA against the active metabolite (active interferon beta 1a portion) of peginterferon beta-1a.
Rows 7-10:Show the screening, confirmation and quantification of ADA against the PEG epitope portion of peginterferon beta-1a.



Dataset2


RowSTUDYIDDOMAINUSUBJIDISSEQISREFID ISTESTCDISTESTISBDAGNTISCATISSCATISORRESISORRESU ISSTRESCISSTRESN ISSTRESUISSPECISMETHODVISITNUMVISITISDTC
ISTSTOPO
 1 ABCIS ABC-007 1 A1

ADA_BAB

Binding Antidrug Antibody

ACTIVE INTERFERON BETA 1A PORTION OF PEGINTERFERON BETA1A

ANTIDRUG ANTIBODIES

 
HUMORAL IMMUNITYPOSITIVE 
POSITIVE 

SERUM 

IMMUNOASSAY

1VISIT 12017-07-27
SCREEN

 2

 ABCIS ABC-0072 A1

ADA_BAB

Binding Antidrug Antibody

PEG PORTION OF PEGINTERFERON BETA1A

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITYPOSITIVE 
POSITIVE 

SERUM ELISA1VISIT 12017-07-27
SCREEN
 3 ABCIS ABC-007  A1ADA_BAB Binding Antidrug Antibody PEG PORTION of PEGINTERFERON BETA1AANTIDRUG ANTIBODIES HUMORAL IMMUNITYNEGATIVE 
NEGATIVE 

 SERUMELISAVISIT 1 2017-07-27 

CONFIRM

 4 ABC ISABC-007  A1ADA_NAB Neutralizing Antidrug Antibody PEGINTERFERON BETA1AANTIDRUG ANTIBODIES HUMORAL IMMUNITYPOSITIVE 
POSITIVE 

SERUM REPORTER GENE IMMUNOASSAY1VISIT 1 2017-07-27 
SCREEN
 5 ABC ISABC-007  A1ADA_NAB Neutralizing Antidrug Antibody PEGINTERFERON BETA1AANTIDRUG ANTIBODIES HUMORAL IMMUNITY 4.7titer4.7 4.7titerSERUM REPORTER GENE IMMUNOASSAY1VISIT 1 2017-07-27 
QUANTIFY
 6 ABCIS ABC-0086 V4

ADA_BAB

Binding Antidrug Antibody

ACTIVE INTERFERON BETA 1A PORTION OF PEGINTERFERON BETA1A

ANTIDRUG ANTIBODIES

 
HUMORAL IMMUNITYNEGATIVE 
NEGATIVE 

SERUM 

IMMUNOASSAY

1VISIT 12017-08-27
SCREEN

 7

 ABCIS ABC-0087 V4

ADA_BAB

Binding Antidrug Antibody

PEG PORTION OF PEGINTERFERON BETA1A

ANTIDRUG ANTIBODIES 

HUMORAL IMMUNITYPOSITIVE 
POSITIVE 

SERUM ELISA1VISIT 12017-08-27
SCREEN
 8 ABCIS ABC-008  V4ADA_BAB Binding Antidrug Antibody PEG PORTION OF PEGINTERFERON BETA1A ANTIDRUG ANTIBODIES HUMORAL IMMUNITYPOSITIVE 
POSITIVE 

 SERUMELISAVISIT 1 2017-08-27 

CONFIRM

 9 ABC ISABC-008  V4ADA_BAB Binding Antidrug Antibody PEG PORTION OF PEGINTERFERON BETA1A ANTIDRUG ANTIBODIES HUMORAL IMMUNITY40titer40 40titerSERUM ELISA1VISIT 1 2017-08-27 
QUANTIFY



Nsvmeta
DomainIS


VariableLabelTypeRoleOrigin
ISTSTOPO Test Operational ObjectivetextNon-Standard Record QualifierCRF



Example 5 - Autoimmune Disease Diagnosis

The example below shows how to represent autoantibody data.

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Rows 1-2:Show the screening and quantification of Antinuclear Antibodies, and ISBDAGNT is not populated. This is because, If an antibody test has multiple, unclearly defined/described targets, a pre-coordinated ISTEST should be created and ISBDAGNT should not be populated. In this case extractable nuclear antigens consist of >100 different soluble cytoplasmic and nuclear antigens, the ISBDAGNT variable cannot clearly and appropriately represent the target(s) of this antibody test, therefore the pre-cooirdinated ISTEST of Antinuclear Antibodies is used.
Rows 3-8:Show the screening and quantification of various Sjogren's Syndrome specific autoantibodies.



Dataset2


RowSTUDYIDDOMAINUSUBJIDISSEQISREFIDISGRPIDISTESTCDISTESTISBDAGNTISORRESISORRESUISSTRESCISSTRESNISSTRESUISSPECISMETHODVISITNUMVISITISDTC
ISTSTOPO
1XYZISXYZ12341192837461ANAAntinuclear Antibodies
POSITIVE
POSITIVE

SERUMMULTIPLEXED BEAD BASED IMMUNOASSAY1SCREENING2018-06-20
SCREEN
2XYZISXYZ12342192837461ANAAntinuclear Antibodies
340titerPOSITIVE340titerSERUMMULTIPLEXED BEAD BASED IMMUNOASSAY1SCREENING2018-06-20
QUANTIFY
3XYZISXYZ12341192837462ATABBinding Autoantibody

SJOGRENS SS-A60

POSITIVE
POSITIVE

SERUMMULTIPLEXED BEAD BASED IMMUNOASSAY1SCREENING2018-06-20
SCREEN
4XYZISXYZ12342192837462ATABBinding Autoantibody

SJOGRENS SS-A60

181AU/mL181181AU/mLSERUMMULTIPLEXED BEAD BASED IMMUNOASSAY1SCREENING2018-06-20
QUANTIFY
5XYZISXYZ12343192837463ATABBinding AutoantibodySJOGRENS SS-A52POSITIVE
POSITIVE

SERUMMULTIPLEXED BEAD BASED IMMUNOASSAY1SCREENING2018-06-20
SCREEN
6XYZISXYZ12344192838823ATABBinding Autoantibody

SJOGRENS SS-A52

51AU/mL5151AU/mLSERUMMULTIPLEXED BEAD BASED IMMUNOASSAY1SCREENING2018-06-20
QUANTIFY
7XYZISXYZ12345192838824ATABBinding AutoantibodySJOGRENS SS-BPOSITIVE
POSITIVE

SERUMMULTIPLEXED BEAD BASED IMMUNOASSAY1SCREENING2018-06-20
SCREEN
8XYZISXYZ12346192838824ATABBinding Autoantibody

SJOGRENS SS-B

169AU/mL169169AU/mLSERUMMULTIPLEXED BEAD BASED IMMUNOASSAY1SCREENING2018-06-20
QUANTIFY



Nsvmeta
DomainIS


VariableLabelTypeRoleOrigin
ISTSTOPOTest Operational ObjectivetextNon-Standard Record QualifierCRF




Example 6 - Vaccine Studies

The example below shows how to represent data about vaccine-induced immunological responses, as well immunological data collected during the trial but are not germane to the study vaccine.

...

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Rows 1-2:

Show the screening and quantification of "Binding Microbial-induced IgG Antibody" against the Human Respiratory Syncytial virus (RSV)-epitope B at baseline, prior to the administration of the study vaccine. The ISBDAGNT value of "HUMAN RESPIRATORY SYNCYTIAL VIRUS-EPITOPE B", is the immunogenic target in the study vaccine that could potentially stimulate the production of antibodies. Note the ISCAT value here is STUDY VACCINE-INDUCED IMMUNOGENICITY, even though at this point, study vaccine has not been administered to the subject - this is done purposefully to enable the grouping of baseline and treatment measurements.

Rows 3-4:Show the screening and quantification of "Binding Microbial-induced IgG Antibody" against the Influenza A virus at baseline. Co-infection of the Human Respiratory Syncytial virus and Influenza A virus is commonly observed in patients hence baseline anti-Influenza A antibody is also measured to see if the subject suffers from influenza infection as well. Please note, since Influenza A is NOT the immunogenic target of interest in the RSV Vaccine Study, the ISCAT is therefore populated with the value "HISTORICAL INFECTION OR PREVIOUS VACCINATION".

Rows 5-6:

Show the titer of "Binding Microbial-induced IgG Antibody" against the RSV-epitope B post-vaccination at visit 1 and 2. These two records show the antibody titers had increased post-vaccination, presumably due to the stimulation from the RSV study vaccine. Note the ISCAT is populated with the value "VACCINE-RELATED IMMUNOGENICITY".



Dataset2


Row

STUDYID

DOMAIN

USUBJID

ISSEQ

ISREFID

ISGRPID

ISTESTCD

ISTEST

ISBDAGNT

ISTSTDTLISTSTOPO

ISCAT

ISSCAT

ISORRES

ISORRESU

ISSTRESC

ISSTRESN

ISSTRESU

ISSPEC

ISMETHOD

VISITNUM

VISIT

ISDTC


ISTSTOPO

1

RSV1230

IS

RSV1230-011

1

13668

1


Binding Microbial-induced IgG Antibody

HUMAN RESPIRATORY SYNCYTIAL VIRUS-EPITOPE B

VACCINE-RELATED IMMUNOGENICITYHUMORAL IMMUNITY

POSITIVE


POSITIVE



SERUM

ELISA

1

BASELINE

2017-05-27


SCREEN

2

RSV1230

IS

RSV1230-011

2

13668

1

Binding Microbial-induced IgG Antibody

HUMAN RESPIRATORY SYNCYTIAL VIRUS-EPITOPE B

VACCINE-RELATED IMMUNOGENICITY

HUMORAL IMMUNITY

25

titer

25

25titer

SERUM

ELISA

1

BASELINE

2017-05-27


QUANTIFY

3

RSV1230

IS

RSV1230-011

1

13668

2


Binding Microbial-induced IgG Antibody

INFLUENZA A VIRUS

HISTORICAL INFECTION OR PREVIOUS VACCINATIONHUMORAL IMMUNITYPOSITIVE
POSITIVE

SERUM

ELISA

1

BASELINE

2017-05-27


SCREEN

4

RSV1230

IS

RSV1230-011

2

13668

2


Binding Microbial-induced IgG Antibody

INFLUENZA A VIRUS

HISTORICAL INFECTION OR PREVIOUS VACCINATIONHUMORAL IMMUNITY120titer120120titer

SERUM

ELISA

1

BASELINE

2017-05-27


QUANTIFY

5

RSV1230

IS

RSV1230-011

1

13668



Binding Microbial-induced IgG Antibody

HUMAN RESPIRATORY SYNCYTIAL VIRUS-EPITOPE B

VACCINE-RELATED IMMUNOGENICITY

HUMORAL IMMUNITY

90

titer

90

90

titer

SERUM

ELISA

2

VISIT 1

2017-07-27


QUANTIFY

6RSC1230IS

RSV1230-011

213668

Binding Microbial-induced IgG Antibody

HUMAN RESPIRATORY SYNCYTIAL VIRUS-EPITOPE B

VACCINE-RELATED IMMUNOGENICITY

HUMORAL IMMUNITY500titer500500titer

SERUM

ELISA

3VISIT 22017-08-27

QUANTIFY



Nsvmeta
DomainIS


VariableLabelTypeRoleOrigin
ISTSTOPO Test Operational ObjectivetextNon-Standard Record QualifierCRF



Example 7: Testing of Antibody-secreting Cells

Traditional methods such as ELISA that monitor humoral immune responses after immunization or infection typically only quantify specific antibody titers in serum. These methods do not provide any information about the actual number and location of the immune cells that secrete antibodies or cytokines.

...


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Row 1:

Shows the total number of IgG antibody secreting cells (ASCs) from a subject’s blood sample. In this case, ISTEST = Antibody-secreting Cells, where the entity secreted by the cells in ISTEST is represented by the variable, Secreted Molecule by Cells/ISSCMBCL. 

Row 2:

Shows the number of H1 specific IgG ASCs from the same subject’s blood sample. In this case, ISTEST = Antibody-secreting Cells, where the entity secreted by the cells in ISTEST is in ISSCMBCL as "IgG antibody specific to H1 antigen".

Row 3:

Shows the number of H3 specific IgG ASCs from the same subject’s blood sample. In this case, ISTEST = Antibody-secreting Cells, where the entity secreted by the cells in ISTEST is in ISSCMBCL as "IgG antibody specific to H3 antigen".



Dataset2


Row

STUDYID

DOMAIN

USUBJID

ISSEQ

ISREFID

ISTESTCD

ISTEST

ISSCMBCL

ISCATISSCAT

ISORRES

ISORRESU

ISSTRESC

ISSTRESN

ISSTRESU

ISSPEC

ISMETHOD

ISDTC

1

INFL456

IS

INF02-01

1

SAMPBL0201

ABSCCL

Antibody-secreting Cells

TOTAL IGG ANTIBODY

VACCINE-RELATED IMMUNOGENICITY

HUMORAL IMMUNITY

2019

SFC/10^6 PBMC

2019

2019

SFC/10^6 PBMC

PERIPHERAL BLOOD MONONUCLEAR CELL

ELISPOT

2011-08-08

2

INFL456

IS

INF02-01

2

SAMPBL0201

ABSCCL

Antibody-secreting Cells

INFLUENZA H1-SPECIFIC IGG ANTIBODY

VACCINE-RELATED IMMUNOGENICITY

HUMORAL IMMUNITY

626

SFC/10^6 PBMC

626

626

SFC/10^6 PBMC

PERIPHERAL BLOOD MONONUCLEAR CELL

ELISPOT

2011-08-08

3

INFL456

IS

INF02-01

3

SAMPBL0201

ABSCCL

Antibody-secreting Cells

INFLUENZA H3-SPECIFIC IGG ANTIBODY

VACCINE-RELATED IMMUNOGENICITY

HUMORAL IMMUNITY

592

SFC/10^6 PBMC

592

592

SFC/10^6 PBMC

PERIPHERAL BLOOD MONONUCLEAR CELL

ELISPOT

2011-08-08




Example 8: Testing of Cytokine-secreting Cells

The example below shows data from the vaccine study for Respiratory Syncytial Virus (RSV) where the subject is being vaccinated with a viral vector containing RSV Epitope B. Peripheral blood mononuclear cells are isolated from the the subject and are tested before (as baseline) and after vaccination in order to investigate whether the circulating PBMCs produce increasing amounts of Interferon gamma after re-stimulating with control or RSV-Epitope B in vitro.

The example below shows how to represent the quantification of cytokine-secreting cells as the number of spots per million peripheral blood mononuclear cells (PBMC) as determined by T-Cell ELISpot from a vaccine trial.

Dataset wrap
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Rowcaps


Rows 1-2:

Show the measurement of Cytokine-secreting Cells (ISTEST) at baseline after stimulation with placebo (row 1) or RSV Epitope B (Row 2) respectively. The type of cytokine-secreting cells that is measured in this record produces Interferon Gamma, which is represented by the ISSCMBCL variable.

Rows 3-4:

Show the measurement of Cytokine-secreting Cells (ISTEST) at Visit 1 after stimulation with placebo (row 3) or RSV Epitope B (row 4) respectively. The type of cytokine-secreting cells that is measured in this record produces Interferon Gamma, which is represented by the ISSCMBCL variable.



Dataset2


Row

STUDYID

DOMAIN

USUBJID

ISSEQ

ISREFID

ISTESTCD

ISTEST

ISSCMBCL

ISTSTDTLISTSTOPOISCATISSCAT

ISORRES

ISORRESU

ISSTRESC

ISSTRESN

ISSTRESU

ISSPEC

ISMETHOD

VISITNUMVISIT

ISDTC


ISAGSTIM

1

RSV1230

IS

RSV1230-011

1

13668

CYKSCCL

Cytokine-secreting Cells

INTERFERON GAMMA

VACCINE-RELATED IMMUNOGENICITYCELLULAR IMMUNITY

5.1

SFC/10^6 PBMC

5.1

5.1

SFC/10^6 PBMC

PERIPHERAL BLOOD MONONUCLEAR CELL

ELISPOT

1BASELINE

2017-05-27


NEGATIVE CONTROL

2

RSV1230

IS

RSV1230-011

2

13668

CYKSCCL

Cytokine-secreting Cells

INTERFERON GAMMA

VACCINE-RELATED IMMUNOGENICITYCELLULAR IMMUNITY

40.5

SFC/10^6 PBMC

40.5

40.5

SFC/10^6 PBMC

PERIPHERAL BLOOD MONONUCLEAR CELL

ELISPOT

1BASELINE

2017-05-27


RSV-EPITOPE B

3

RSV1230

IS

RSV1230-011

3

13668

CYKSCCL

Cytokine-secreting Cells

INTERFERON GAMMA

VACCINE-RELATED IMMUNOGENICITYCELLULAR IMMUNITY

6.3

SFC/10^6 PBMC

6.3

6.3

SFC/10^6 PBMC

PERIPHERAL BLOOD MONONUCLEAR CELL

ELISPOT

2VISIT 1

2017-08-27


NEGATIVE CONTROL
4RSV1230ISRSV1230-011413668CYKSCCLCytokine-secreting CellsINTERFERON GAMMA

VACCINE-RELATED IMMUNOGENICITYCELLULAR IMMUNITY260.5

SFC/10^6 PBMC

260.5260.5

SFC/10^6 PBMC

PERIPHERAL BLOOD MONONUCLEAR CELL

ELISPOT2VISIT 12017-08-27
RSV-EPITOPE B



Nsvmeta
DomainIS


VariableLabelTypeRoleOrigin
ISAGSTIMAntigen StimulationtextNon-Standard Record QualifierCRF



Example 9 - Microneutralization Assay

In vaccine studies, microneutralization assays are commonly used in vitro assays to quantify viral-specific neutralizing antibodies in the subject’s specimen that can block viral infection in vitro, and so provide output of vaccine efficacy.  

...

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Dataset2


Row

STUDYID

DOMAIN

USUBJID

ISSEQ

ISREFID

ISTESTCD

ISTEST

ISBDAGNT

ISTSTDTLISTSTOPOISCATISSCAT

ISORRES

ISORRESU

ISSTRESC

ISSTRESN

ISSTRESU

ISSPEC

ISMETHOD

VISITNUMVISIT

ISDTC

1

RSV1230

IS

RSV1230-011

1

13668


Neutralizing Binding Microbial-induced Antibody

RESPIRATORY SYNCYTIAL VIRUSNEUTRALIZING TITER 50%
VACCINE-RELATED IMMUNOGENICITYHUMORAL IMMUNITY

40

titer

40

40

titer

SERUM

MICRONEUTRALIZATION ASSAY

1BASELINE

2017-05-27

2

RSV1230

IS

RSV1230-011

2

13668


Neutralizing Binding Microbial-induced Antibody

RESPIRATORY SYNCYTIAL VIRUS

NEUTRALIZING TITER 50%
VACCINE-RELATED IMMUNOGENICITYHUMORAL IMMUNITY

80

titer

80

80

titer

SERUM

MICRONEUTRALIZATION ASSAY

2VISIT 1

2017-07-27

3

RSV1230

IS

RSV1230-011

3

13668


Neutralizing Binding Microbial-induced Antibody

RESPIRATORY SYNCYTIAL VIRUS

NEUTRALIZING TITER 50%
VACCINE-RELATED IMMUNOGENICITYHUMORAL IMMUNITY

200

titer

200

200

titer

SERUM

MICRONEUTRALIZATION ASSAY

3VISIT 2

2017-08-27



Example 10 - Opsonophagocytic Killing Assay

In vaccine trials, the opsonophagocytic killing (OPK) assay is used as a correlate for protection to measure the "functional capacities" of vaccine-induced antibodies. This in vitro assay aids selecting promising vaccines by demonstrating whether the vaccine-induced antibodies drive efficient complement deposition and subsequent opsonophagocytic killing. 

...

Dataset wrap
Nameis


Dataset2


Row

STUDYID

DOMAIN

USUBJID

ISSEQ

ISREFID

ISTESTCD

ISTEST

ISBDAGNT

ISTSTDTLISTSTOPOISCATISSCAT

ISORRES

ISSTRESC

ISSTRESN

ISSPEC

ISMETHOD

VISITNUMVISIT

ISDTC

1

RSV1230

IS

RSV1230-011

1

13668


Functional Binding Microbial-induced Antibody

ESCHERICHIA COLI – EPITOPE XOPSONIZATION INDEX
VACCINE-RELATED IMMUNOGENICITYHUMORAL IMMUNITY

1

1

1

SERUM

OPSONOPHAGOCYTIC KILLING ASSAY

1BASELINE

2017-05-27

2

RSV1230

IS

RSV1230-011

2

13668


Functional Binding Microbial-induced Antibody

ESCHERICHIA COLI – EPITOPE X

OPSONIZATION INDEX
VACCINE-RELATED IMMUNOGENICITYHUMORAL IMMUNITY

3

3

3

SERUM

OPSONOPHAGOCYTIC KILLING ASSAY

2VISIT 1

2017-07-27

3

RSV1230

IS

RSV1230-011

3

13668


Functional Binding Microbial-induced Antibody

ESCHERICHIA COLI – EPITOPE X

OPSONIZATION INDEX
VACCINE-RELATED IMMUNOGENICITYHUMORAL IMMUNITY

5

5

5

SERUM

OPSONOPHAGOCYTIC KILLING ASSAY

3VISIT 2

2017-09-27




Example 11 - Hemagglutination Inhibition Assay

The OI data below shows how to represent the various taxanomic naming levels of Influenza A virus (A/duck/Hong Kong/33/1976(H10N1)).

...