Evidence map›Paper›PMID 29285931›Full record

ReviewBioconjugate chemistry2018

Enzymes as Immunotherapeutics.

Shaheen A Farhadi, Evelyn Bracho-Sanchez, Sabrina L Freeman, Benjamin G Keselowsky, Gregory A Hudalla

Abstract readReview
In one paragraph

Review in Bioconjugate chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Production and Purification of Therapeutic Enzymes.Advances in experimental medicine and biology · 2019
    Review
  8. Article
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Shaheen A FarhadiJ. Crayton Pruitt Family Department of Biomedical Engineering, College of Engineering , University of Florida , Gainesville , Florida 32611 , United States.
Evelyn Bracho-SanchezJ. Crayton Pruitt Family Department of Biomedical Engineering, College of Engineering , University of Florida , Gainesville , Florida 32611 , United States.
Sabrina L FreemanJ. Crayton Pruitt Family Department of Biomedical Engineering, College of Engineering , University of Florida , Gainesville , Florida 32611 , United States.
Benjamin G KeselowskyJ. Crayton Pruitt Family Department of Biomedical Engineering, College of Engineering , University of Florida , Gainesville , Florida 32611 , United States.ORCID 0000-0001-6474-7769
Gregory A HudallaJ. Crayton Pruitt Family Department of Biomedical Engineering, College of Engineering , University of Florida , Gainesville , Florida 32611 , United States.

Funding

Tolerogenic dual microparticle system for treatment of multiple sclerosisR01AI133623 · NIAID · UNIVERSITY OF FLORIDA · PI AVRAM, DORINA, KESELOWSKY, BENJAMIN GEORGE · 2017 to 2021
$2.6M
Tissue-Targeted Enzyme for Localized Tryptophan Catabolism to Direct Subcutaneous and Oral Mucosal Inflammatory ResponsesR01DE027301 · NIDCR · UNIVERSITY OF FLORIDA · PI KESELOWSKY, BENJAMIN GEORGE · 2017 to 2020
$2.0M
Biomaterial Delivery System for Type 1 Diabetes VaccineR01DK098589 · NIDDK · UNIVERSITY OF FLORIDA · PI KESELOWSKY, BENJAMIN GEORGE · 2014 to 2017
$1.5M
Supramolecular hydrogels for localized delivery of immunomodulatory enzymesR21EB024762 · NIBIB · UNIVERSITY OF FLORIDA · PI HUDALLA, GREGORY · 2017 to 2019
$591k
Modular Nanomedicines Based on Heterogeneous Fusion Protein Co-AssemblyR03EB019684 · NIBIB · UNIVERSITY OF FLORIDA · PI HUDALLA, GREGORY · 2015 to 2016
$141k
NIAID NIH HHS R01 AI133623NIBIB NIH HHS R03 EB019684NIBIB NIH HHS R21 EB024762NIDCR NIH HHS R01 DE027301NIDDK NIH HHS R01 DK098589
6 · The paper itself

Abstract

Enzymes are attractive as immunotherapeutics because they can catalyze shifts in the local availability of immunostimulatory and immunosuppressive signals. Clinical success of enzyme immunotherapeutics frequently hinges upon achieving sustained biocatalysis over relevant time scales. The time scale and location of biocatalysis are often dictated by the location of the substrate. For example, therapeutic enzymes that convert substrates distributed systemically are typically designed to have a long half-life in circulation, whereas enzymes that convert substrates localized to a specific tissue or cell population can be more effective when designed to accumulate at the target site. This Topical Review surveys approaches to improve enzyme immunotherapeutic efficacy via chemical modification, encapsulation, and immobilization that increases enzyme accumulation at target sites or extends enzyme half-life in circulation. Examples provided illustrate "replacement therapies" to restore deficient enzyme function, as well as "enhancement therapies" that augment native enzyme function via supraphysiologic doses. Existing FDA-approved enzyme immunotherapies are highlighted, followed by discussion of emerging experimental strategies such as those designed to enhance antitumor immunity or resolve inflammation.

Indexed as

alpha-GalactosidaseAnimalsAnti-Inflammatory AgentsAntineoplastic AgentsAsparaginaseBiocatalysisEnzymes, ImmobilizedEnzyme TherapyFabry DiseaseGaucher DiseaseGlucosylceramidaseGlycosylationHumansImmunoconjugatesImmunotherapyInflammationalpha-GalactosidaseAnti-Inflammatory AgentsAntineoplastic AgentsAsparaginaseEnzymes, ImmobilizedGlucosylceramidaseImmunoconjugates

Identifiers

PMID29285931
PMCPMC5993548

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.