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How Engineered Antibodies Target TGF-beta Proteins to Fight Cancer

This patent describes specific engineered antibodies, made from mouse and human parts, designed to block TGF-beta proteins to help treat various cancers like breast or lung cancer.

Granted 2009ExpiredExpired 2025Owned by Genentech IncInvented by Leonard G. Presta, Napoleone Ferrara, Weiguang Mao + 3 more

Original patent title: “Humanized anti-TGF-beta antibodies

Plain-English explanation by SahiLast reviewed · June 15, 2026

This patent describes specific engineered antibodies, made from mouse and human parts, designed to block TGF-beta proteins to help treat various cancers like breast or lung cancer. Granted to Genentech Inc in 2009 with 27 claims and 756 forward citations.

Key facts

Patent numberUS 7527791
StatusExpired
FieldBiotech & Medicine
AssigneeGenentech Inc
InventorsLeonard G. Presta, Napoleone Ferrara, Weiguang Mao and 3 others
Filed2005
Granted2009
Claims27
Times cited756
LitigationNone on record
Value · $219K$702KModest

Coverage

What does this patent actually cover?

This patent claimsclaimsThe numbered statements at the end of a patent that legally define what the inventor owns.Read more → a specific type of 'humanized antibody' designed to bind to and block TGF-beta proteins (TGF-beta1, TGF-beta2, or TGF-beta3). A humanized antibody is engineered to combine the target-binding parts of a non-human antibody with the structural parts of a human antibody, making it less likely for a human body to reject. Specifically, the antibody has a variable heavy (VH) domain that includes non-human hypervariable regions (like those from SEQ ID NO: 21, 23, and 43) inserted into a human framework region (like SEQ ID NO:6). This human framework region also has specific amino acid changes, or 'substitutions,' at certain positions (e.g., 48, 49, 68, and 72). The antibody also includes specific variable light (VL) domain complementarity-determining-region (CDR) residues (like SEQ ID NO:18, 19, and 20). These antibodies are intended for treating TGF-beta disorders, such as colo-rectal cancer, melanoma, or cancers of the breast, prostate, or lung, as mentioned in claimclaimA numbered sentence at the end of a patent that legally defines what the inventor owns. The most important section.Read more → 23.

The gap

What does this patent NOT cover?

  • Does not cover antibodies that are entirely mouse-derived or entirely human-derived, as it specifically claimsclaimsThe numbered statements at the end of a patent that legally define what the inventor owns.Read more → a 'humanized' antibody combining non-human hypervariable regions with a human framework.
  • Does not cover antibodies that bind to proteins other than TGF-beta1, TGF-beta2, or TGF-beta3, as specified in claimclaimA numbered sentence at the end of a patent that legally defines what the inventor owns. The most important section.Read more → 1.
  • Does not cover humanized antibodies with different specific amino acid sequences in their hypervariable or framework regions than those listed (e.g., SEQ ID NO:6, 18, 19, 20, 21, 23, 43) or different framework substitutions.
  • Does not cover small molecule drugs or other types of biologics that are not antibodies or antibody fragments (like Fab fragments, as in claimclaimA numbered sentence at the end of a patent that legally defines what the inventor owns. The most important section.Read more → 19).
  • Does not cover methods of treating disorders that are not related to TGF-beta, even if they are cancers.

These exclusions are unique to PatentBrief — derived from the actual claim language, not patent-office boilerplate.

What made this novel

The cleverness lies in identifying the precise amino acid changes, or 'substitutions,' within the human framework regions of the antibody (e.g., at positions 48, 49, 68, and 72 as detailed in claimsclaimsThe numbered statements at the end of a patent that legally define what the inventor owns.Read more → 1-13). These specific changes are crucial for ensuring the humanized antibody maintains its strong ability to bind to TGF-beta while also being recognized as 'self' by the human immune system, thus reducing unwanted side effects.

Humanized anti-TGF-beta antibo…(Primary claim)biotechpharmaceuticaloncologyimmunology

Schematic visualization of the patent's claim structure. Hand-drawn diagrams in progress for each landmark patent.

Where you've seen this

Real-world examples

01

Humanized antibody therapies for various cancers

02

Oncology drugs targeting growth factor pathways

03

Antibodies in clinical trials for fibrosis, where TGF-beta also plays a role

Why it matters

The bigger picture

Humanized antibodies were a major step in making antibody-based drugs safe and effective for people, as earlier non-human antibodies often caused severe immune reactions. TGF-beta is a protein that can promote tumor growth and spread in many cancers, so blocking it with an antibody like the one described here offers a way to potentially slow down or stop cancer progression. Genentech, the assigneeassigneeThe entity that owns the patent — usually the inventor's employer or a company.Read more →, is a leading biotechnology company known for developing many successful antibody therapies for cancer.

Filed

March 31, 2005

Granted

May 5, 2009

Market context

Who's building on this

Companies in this space

Genentech, now part of Roche, continues to be a major player in developing antibody therapies, including those for cancer. Other large pharmaceutical and biotechnology companies like AstraZeneca, Bristol Myers Squibb, and Merck are also actively researching and developing antibodies that target the TGF-beta pathway for various diseases, including oncology and fibrotic conditions.

Market impact

The development of humanized antibodies, generally, transformed the pharmaceutical industry by enabling the creation of highly specific and effective biologic drugs with reduced side effects. This patent specifically contributes to the field of targeted cancer therapies by providing a blueprint for antibodies that interfere with the TGF-beta pathway, a known contributor to tumor growth and immune suppression. This approach has led to numerous clinical trials and the development of new drug candidates aimed at modulating this pathway in cancer and other diseases.

Claim 1 — Plain English

What this patent covers

This patent claims a specific type of 'humanized antibody' designed to bind to and block TGF-beta proteins (TGF-beta1, TGF-beta2, or TGF-beta3). A humanized antibody is engineered to combine the target-binding parts of a non-human antibody with the structural parts of a human antibody, making it less likely for a human body to reject. Specifically, the antibody has a variable heavy (VH) domain that includes non-human hypervariable regions (like those from SEQ ID NO: 21, 23, and 43) inserted into a human framework region (like SEQ ID NO:6). This human framework region also has specific amino acid changes, or 'substitutions,' at certain positions (e.g., 48, 49, 68, and 72). The antibody also includes specific variable light (VL) domain complementarity-determining-region (CDR) residues (like SEQ ID NO:18, 19, and 20). These antibodies are intended for treating TGF-beta disorders, such as colo-rectal cancer, melanoma, or cancers of the breast, prostate, or lung, as mentioned in claim 23.

The clever bit

The cleverness lies in identifying the precise amino acid changes, or 'substitutions,' within the human framework regions of the antibody (e.g., at positions 48, 49, 68, and 72 as detailed in claims 1-13). These specific changes are crucial for ensuring the humanized antibody maintains its strong ability to bind to TGF-beta while also being recognized as 'self' by the human immune system, thus reducing unwanted side effects.

What it does not cover

  • Does not cover antibodies that are entirely mouse-derived or entirely human-derived, as it specifically claims a 'humanized' antibody combining non-human hypervariable regions with a human framework.
  • Does not cover antibodies that bind to proteins other than TGF-beta1, TGF-beta2, or TGF-beta3, as specified in claim 1.
  • Does not cover humanized antibodies with different specific amino acid sequences in their hypervariable or framework regions than those listed (e.g., SEQ ID NO:6, 18, 19, 20, 21, 23, 43) or different framework substitutions.
  • Does not cover small molecule drugs or other types of biologics that are not antibodies or antibody fragments (like Fab fragments, as in claim 19).
  • Does not cover methods of treating disorders that are not related to TGF-beta, even if they are cancers.

Patent timeline

Filing

Application submitted to the patent office

Publication

Application published, typically 18 months after filing

Grant

Patent officially issued

PatentBrief Score

Impact Score

High impact

Citation count

40/40

Highly cited

Claim breadth

18/20

Very broad protection

Recency

5/20

Granted 10–20 years ago

Assignee scale

20/20

Major company or institution

PatentBrief Impact Score — based on citation count, claim breadth, recency, and assignee scale. Not a legal assessment.

Heuristic Value Estimate

What this patent might be worth

Modest

$219K$702K

Midpoint $439K · expired or expiring · industry ×3.0

Adjust inputs →

Heuristic only — blends forward/backward citation counts, claim scope, time remaining, litigation history, and CPC-derived industry baseline. Real valuations need a professional appraisal.

The original legal language

Original claims

27 claims as filed with the patent office.

Concepts involved

ClaimPrior artNon-obviousnessNoveltySpecificationAssigneePatent term

Citations

Patent lineage

Cites earlier patents

215

earlier patents this invention cites as foundations

View prior art →

Cited by later patents

756

later patents that build on this invention

View patents →

Cite this patent

Presta, L. G., Ferrara, N., Mao, W., Filvaroff, E. H., Adams, C. W., & Tejada, M. L. (2009). How Engineered Antibodies Target TGF-beta Proteins to Fight Cancer (U.S. Patent No. 7,527,791). U.S. Patent and Trademark Office. https://patentbrief.org/patent/us/7527791/ipilimumab-yervoy

Auto-generated from the patent record. Double-check author order and the issue date against the official USPTO document before submitting.

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Common Questions

Frequently Asked Questions

What does How Engineered Antibodies Target TGF-beta Proteins to Fight Cancer cover?

This patent describes specific engineered antibodies, made from mouse and human parts, designed to block TGF-beta proteins to help treat various cancers like breast or lung cancer.

Who owns patent US 7527791?

Genentech Inc owns this patent, granted in 2009.

When does this patent expire?

This patent is expected to expire on May 5, 2029, when the invention enters the public domain.

What is patent US 7527791 cited by?

This patent has been cited by 756 later patents that build on its ideas.

What problem does this patent solve?

Humanized antibodies were a major step in making antibody-based drugs safe and effective for people, as earlier non-human antibodies often caused severe immune reactions. TGF-beta is a protein that can promote tumor growth and spread in many cancers, so blocking it with an antibody like the one described here offers a way to potentially slow down or stop cancer progression. Genentech, the assignee, is a leading biotechnology company known for developing many successful antibody therapies for cancer.

What does this patent NOT cover?

Does not cover antibodies that are entirely mouse-derived or entirely human-derived, as it specifically claims a 'humanized' antibody combining non-human hypervariable regions with a human framework.

Same assignee

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Last reviewed: June 15, 2026 · PatentBrief is not a law firm and this is not legal advice.